SNP Links for Gene (Select 7738) - SNP

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Select item 14915864881.

rs1491586488 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:27422159 (GRCh38)
6:27389939 (GRCh37)
Canonical SPDI:: NC_000006.12:27422159:G:GG
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000006.12:g.27422160dup, NC_000006.11:g.27389939dup, NG_052614.1:g.55959dup

Select item 14915559292.

rs1491555929 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 6:27423912 (GRCh38)
6:27391692 (GRCh37)
Canonical SPDI:: NC_000006.12:27423912:C:CC
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
HGVS:: NC_000006.12:g.27423913dup, NC_000006.11:g.27391692dup, NG_052614.1:g.54206dup

Select item 14915445823.

rs1491544582 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>-,GAGA [Show Flanks]
Chromosome:: 6:27422164 (GRCh38)
6:27389943 (GRCh37)
Canonical SPDI:: NC_000006.12:27422162:AGA:A,NC_000006.12:27422162:AGA:AGAGA
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AGAGA=0./0 (ALFA)
-=0.00006/2 (GnomAD)
HGVS:: NC_000006.12:g.27422164_27422165del, NC_000006.12:g.27422164_27422165dup, NC_000006.11:g.27389943_27389944del, NC_000006.11:g.27389943_27389944dup, NG_052614.1:g.55955_55956del, NG_052614.1:g.55955_55956dup

Select item 14914956494.

rs1491495649 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA [Show Flanks]
Chromosome:: 6:27409524 (GRCh38)
6:27377303 (GRCh37)
Canonical SPDI:: NC_000006.12:27409520:ACACA:ACA,NC_000006.12:27409520:ACACA:ACACACA
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACA=0./0 (ALFA)
AC=0.000004/1 (TOPMED)
AC=0.000922/127 (GnomAD)
HGVS:: NC_000006.12:g.27409522CA[1], NC_000006.12:g.27409522CA[3], NC_000006.11:g.27377301CA[1], NC_000006.11:g.27377301CA[3], NG_009330.3:g.1926CA[1], NG_009330.3:g.1926CA[3], NG_052614.1:g.68595GT[1], NG_052614.1:g.68595GT[3]

Select item 14914463785.

rs1491446378 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 6:27409521 (GRCh38)
6:27377301 (GRCh37)
Canonical SPDI:: NC_000006.12:27409521:C:CC
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
C=0.000036/1 (TOMMO)
HGVS:: NC_000006.12:g.27409522dup, NC_000006.11:g.27377301dup, NG_009330.3:g.1926dup, NG_052614.1:g.68597dup

Select item 14914220776.

rs1491422077 has merged into rs1386450207 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,AAA,AAAA,AAAAAA [Show Flanks]
Chromosome:: 6:27442832 (GRCh38)
6:27410611 (GRCh37)
Canonical SPDI:: NC_000006.12:27442830:AAA:A,NC_000006.12:27442830:AAA:AAAA,NC_000006.12:27442830:AAA:AAAAA,NC_000006.12:27442830:AAA:AAAAAAA
Gene:: ZNF184 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000087/1 (TOMMO)
HGVS:: NC_000006.12:g.27442832_27442833del, NC_000006.12:g.27442833dup, NC_000006.12:g.27442832_27442833dup, NC_000006.12:g.27442833_27442834insAAAA, NC_000006.11:g.27410611_27410612del, NC_000006.11:g.27410612dup, NC_000006.11:g.27410611_27410612dup, NC_000006.11:g.27410612_27410613insAAAA, NG_052614.1:g.35287_35288del, NG_052614.1:g.35288dup, NG_052614.1:g.35287_35288dup, NG_052614.1:g.35288_35289insTTTT

Select item 14914095517.

rs1491409551 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:27463918 (GRCh38)
6:27431698 (GRCh37)
Canonical SPDI:: NC_000006.12:27463918::G
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000027/2 (GnomAD)
HGVS:: NC_000006.12:g.27463918_27463919insG, NC_000006.11:g.27431697_27431698insG, NG_052614.1:g.14200_14201insC

Select item 14913406878.

rs1491340687 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->AAGAA
Chromosome:: no mapping
Canonical SPDI:

Select item 14913163209.

rs1491316320 has merged into rs55966783 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAGATCCTGAACACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAATACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAACCACTGAACAGAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAGAAATAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAGATTCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAGGCAATTTAAAAAACTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAATAAAAAAAGCTTTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAATAAAAAGACCCTCTACACAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAATTAAAAAACTTCTGCAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAACTTCAGCAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAATTAAAAAACCTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAATTAAAAAAGCTTATGAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAATTCAGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAAAAATCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAATACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAGAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATTAAAAAACTTTCTAAACAGAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:27458307 (GRCh38)
6:27426086 (GRCh37)
Canonical SPDI:: NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAGATCCTGAACACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCACTGAACAGAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAATAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGATTCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGCAATTTAAAAAACTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAGCTTTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAGACCCTCTACACAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAATTAAAAAACTTCTGCAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAACTTCAGCAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAATTAAAAAACCTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAATTAAAAAAGCTTATGAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAATTCAGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAATCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAATACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAGAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27458295:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATTAAAAAACTTTCTAAACAGAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
A=0.425/17 (GENOME_DK)
HGVS:: NC_000006.12:g.27458307_27458320del, NC_000006.12:g.27458308_27458320del, NC_000006.12:g.27458309_27458320del, NC_000006.12:g.27458312_27458320del, NC_000006.12:g.27458313_27458320del, NC_000006.12:g.27458314_27458320del, NC_000006.12:g.27458315_27458320del, NC_000006.12:g.27458316_27458320del, NC_000006.12:g.27458317_27458320del, NC_000006.12:g.27458318_27458320del, NC_000006.12:g.27458319_27458320del, NC_000006.12:g.27458320del, NC_000006.12:g.27458320dup, NC_000006.12:g.27458319_27458320dup, NC_000006.12:g.27458318_27458320dup, NC_000006.12:g.27458317_27458320dup, NC_000006.12:g.27458316_27458320dup, NC_000006.12:g.27458315_27458320dup, NC_000006.12:g.27458314_27458320dup, NC_000006.12:g.27458313_27458320dup, NC_000006.12:g.27458312_27458320dup, NC_000006.12:g.27458311_27458320dup, NC_000006.12:g.27458310_27458320dup, NC_000006.12:g.27458309_27458320dup, NC_000006.12:g.27458308_27458320dup, NC_000006.12:g.27458307_27458320dup, NC_000006.12:g.27458306_27458320dup, NC_000006.12:g.27458304_27458320dup, NC_000006.12:g.27458303_27458320dup, NC_000006.12:g.27458302_27458320dup, NC_000006.12:g.27458301_27458320dup, NC_000006.12:g.27458300_27458320dup, NC_000006.12:g.27458299_27458320dup, NC_000006.12:g.27458320_27458321insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27458320_27458321insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27458320_27458321insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27458320_27458321insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27458320_27458321insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27458296_27458320A[45]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[43]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[38]TAAAAAGATCCTGAACACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[37]TACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[34]CCACTGAACAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[33]GAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[33]GAAATAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[33]GATTCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[31]GGCAATTTAAAAAACTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[31]TAAAAAAAGCTTTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[31]TAAAAAGACCCTCTACACAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[29]TTAAAAAACTTCTGCAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[28]CTTCAGCAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[28]TTAAAAAACCTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[28]TTAAAAAAGCTTATGAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[28]TTCAGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[27]TAAAAAAAAAATCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[27]TAAAAAAATACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[27]TAAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.27458296_27458320A[27]TTAAAAAACTTTCTAAACAGAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426086_27426099del, NC_000006.11:g.27426087_27426099del, NC_000006.11:g.27426088_27426099del, NC_000006.11:g.27426091_27426099del, NC_000006.11:g.27426092_27426099del, NC_000006.11:g.27426093_27426099del, NC_000006.11:g.27426094_27426099del, NC_000006.11:g.27426095_27426099del, NC_000006.11:g.27426096_27426099del, NC_000006.11:g.27426097_27426099del, NC_000006.11:g.27426098_27426099del, NC_000006.11:g.27426099del, NC_000006.11:g.27426099dup, NC_000006.11:g.27426098_27426099dup, NC_000006.11:g.27426097_27426099dup, NC_000006.11:g.27426096_27426099dup, NC_000006.11:g.27426095_27426099dup, NC_000006.11:g.27426094_27426099dup, NC_000006.11:g.27426093_27426099dup, NC_000006.11:g.27426092_27426099dup, NC_000006.11:g.27426091_27426099dup, NC_000006.11:g.27426090_27426099dup, NC_000006.11:g.27426089_27426099dup, NC_000006.11:g.27426088_27426099dup, NC_000006.11:g.27426087_27426099dup, NC_000006.11:g.27426086_27426099dup, NC_000006.11:g.27426085_27426099dup, NC_000006.11:g.27426083_27426099dup, NC_000006.11:g.27426082_27426099dup, NC_000006.11:g.27426081_27426099dup, NC_000006.11:g.27426080_27426099dup, NC_000006.11:g.27426079_27426099dup, NC_000006.11:g.27426078_27426099dup, NC_000006.11:g.27426099_27426100insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27426099_27426100insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27426099_27426100insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27426099_27426100insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27426099_27426100insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27426075_27426099A[45]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[43]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[38]TAAAAAGATCCTGAACACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[37]TACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[34]CCACTGAACAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[33]GAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[33]GAAATAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[33]GATTCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[31]GGCAATTTAAAAAACTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[31]TAAAAAAAGCTTTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[31]TAAAAAGACCCTCTACACAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[29]TTAAAAAACTTCTGCAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[28]CTTCAGCAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[28]TTAAAAAACCTTCTGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[28]TTAAAAAAGCTTATGAAAAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[28]TTCAGCACAGAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[27]TAAAAAAAAAATCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[27]TAAAAAAATACAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[27]TAAGAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.27426075_27426099A[27]TTAAAAAACTTTCTAAACAGAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_052614.1:g.19810_19823del, NG_052614.1:g.19811_19823del, NG_052614.1:g.19812_19823del, NG_052614.1:g.19815_19823del, NG_052614.1:g.19816_19823del, NG_052614.1:g.19817_19823del, NG_052614.1:g.19818_19823del, NG_052614.1:g.19819_19823del, NG_052614.1:g.19820_19823del, NG_052614.1:g.19821_19823del, NG_052614.1:g.19822_19823del, NG_052614.1:g.19823del, NG_052614.1:g.19823dup, NG_052614.1:g.19822_19823dup, NG_052614.1:g.19821_19823dup, NG_052614.1:g.19820_19823dup, NG_052614.1:g.19819_19823dup, NG_052614.1:g.19818_19823dup, NG_052614.1:g.19817_19823dup, NG_052614.1:g.19816_19823dup, NG_052614.1:g.19815_19823dup, NG_052614.1:g.19814_19823dup, NG_052614.1:g.19813_19823dup, NG_052614.1:g.19812_19823dup, NG_052614.1:g.19811_19823dup, NG_052614.1:g.19810_19823dup, NG_052614.1:g.19809_19823dup, NG_052614.1:g.19807_19823dup, NG_052614.1:g.19806_19823dup, NG_052614.1:g.19805_19823dup, NG_052614.1:g.19804_19823dup, NG_052614.1:g.19803_19823dup, NG_052614.1:g.19802_19823dup, NG_052614.1:g.19823_19824insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.19823_19824insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.19823_19824insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.19823_19824insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.19823_19824insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.19799_19823T[33]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[63]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[30]GT[2]TCAGGATCTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[29]GTTGTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[25]CTGTTCAGTGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[25]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[30]GTTATTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[30]GTAGAATCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[25]CTGTGCAGAAGTTTTTTAAATTGCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[31]GAAAGCTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[27]GT[2]AG[2]GGTCTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[26]GCAGAAGTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[29]GCTGAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[26]CTGTGCAGAAGGTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[25]CTTTTCATAAGCTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[26]CTGTGCTGAATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[32]GTAGATTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[30]GTTGTATTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[25]CTTATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_052614.1:g.19799_19823T[26]CTGTTTAGAAAGTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149130070110.

rs1491300701 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 6:27423915 (GRCh38)
6:27391694 (GRCh37)
Canonical SPDI:: NC_000006.12:27423911:TCTCT:TCT
Gene:: ZNF184 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCT=0.000071/1 (ALFA)
-=0.000034/9 (TOPMED)
-=0.000036/5 (GnomAD)
HGVS:: NC_000006.12:g.27423913CT[1], NC_000006.11:g.27391692CT[1], NG_052614.1:g.54204GA[1]

Select item 149129863111.

rs1491298631 has merged into rs1321698681 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA [Show Flanks]
Chromosome:: 6:27447084 (GRCh38)
6:27414863 (GRCh37)
Canonical SPDI:: NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27447072:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.27447084_27447091del, NC_000006.12:g.27447085_27447091del, NC_000006.12:g.27447086_27447091del, NC_000006.12:g.27447088_27447091del, NC_000006.12:g.27447089_27447091del, NC_000006.12:g.27447090_27447091del, NC_000006.12:g.27447091del, NC_000006.12:g.27447091dup, NC_000006.12:g.27447090_27447091dup, NC_000006.12:g.27447089_27447091dup, NC_000006.11:g.27414863_27414870del, NC_000006.11:g.27414864_27414870del, NC_000006.11:g.27414865_27414870del, NC_000006.11:g.27414867_27414870del, NC_000006.11:g.27414868_27414870del, NC_000006.11:g.27414869_27414870del, NC_000006.11:g.27414870del, NC_000006.11:g.27414870dup, NC_000006.11:g.27414869_27414870dup, NC_000006.11:g.27414868_27414870dup, NG_052614.1:g.31039_31046del, NG_052614.1:g.31040_31046del, NG_052614.1:g.31041_31046del, NG_052614.1:g.31043_31046del, NG_052614.1:g.31044_31046del, NG_052614.1:g.31045_31046del, NG_052614.1:g.31046del, NG_052614.1:g.31046dup, NG_052614.1:g.31045_31046dup, NG_052614.1:g.31044_31046dup

Select item 149129753912.

rs1491297539 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGAAAGAAAGAA [Show Flanks]
Chromosome:: 6:27422163 (GRCh38)
6:27389943 (GRCh37)
Canonical SPDI:: NC_000006.12:27422163:GAAAGAAAGAA:GAAAGAAAGAAGGAAAGAAAGAA
Gene:: ZNF184 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: GAAAGAAAGAAG=0.00007/3 (GnomAD)
HGVS:: NC_000006.12:g.27422164_27422174GAAA[2]GAAGGAAAGAAAGAA[1], NC_000006.11:g.27389943_27389953GAAA[2]GAAGGAAAGAAAGAA[1], NG_052614.1:g.55945_55955TTCT[2]TTCCTTCTTTCTTTC[1]

Select item 149126977313.

rs1491269773 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:27458295 (GRCh38)
6:27426074 (GRCh37)
Canonical SPDI:: NC_000006.12:27458294:TA:
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00076/9 (ALFA)
-=0.00015/4 (GnomAD)
HGVS:: NC_000006.12:g.27458295_27458296del, NC_000006.11:g.27426074_27426075del, NG_052614.1:g.19823_19824del

Select item 149118182014.

rs1491181820 has merged into rs369380634 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAAAA,AAAAAAAA [Show Flanks]
Chromosome:: 6:27442828 (GRCh38)
6:27410607 (GRCh37)
Canonical SPDI:: NC_000006.12:27442826:AAA:A,NC_000006.12:27442826:AAA:AA,NC_000006.12:27442826:AAA:AAAA,NC_000006.12:27442826:AAA:AAAAA,NC_000006.12:27442826:AAA:AAAAAAAA,NC_000006.12:27442826:AAA:AAAAAAAAA
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.28345/4449 (TOMMO)
HGVS:: NC_000006.12:g.27442828_27442829del, NC_000006.12:g.27442829del, NC_000006.12:g.27442829dup, NC_000006.12:g.27442828_27442829dup, NC_000006.12:g.27442829_27442830insAAAAA, NC_000006.12:g.27442829_27442830insAAAAAA, NC_000006.11:g.27410607_27410608del, NC_000006.11:g.27410608del, NC_000006.11:g.27410608dup, NC_000006.11:g.27410607_27410608dup, NC_000006.11:g.27410608_27410609insAAAAA, NC_000006.11:g.27410608_27410609insAAAAAA, NG_052614.1:g.35291_35292del, NG_052614.1:g.35292del, NG_052614.1:g.35292dup, NG_052614.1:g.35291_35292dup, NG_052614.1:g.35292_35293insTTTTT, NG_052614.1:g.35292_35293insTTTTTT

Select item 149113028215.

rs1491130282 has merged into rs1460993712 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>-,GAGA [Show Flanks]
Chromosome:: 6:27422160 (GRCh38)
6:27389939 (GRCh37)
Canonical SPDI:: NC_000006.12:27422158:AGA:A,NC_000006.12:27422158:AGA:AGAGA
Gene:: ZNF184 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: AGAGA=0./0 (ALFA)
HGVS:: NC_000006.12:g.27422160_27422161del, NC_000006.12:g.27422160_27422161dup, NC_000006.11:g.27389939_27389940del, NC_000006.11:g.27389939_27389940dup, NG_052614.1:g.55959_55960del, NG_052614.1:g.55959_55960dup

Select item 149108467716.

rs1491084677 has merged into rs753423028 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 6:27442858 (GRCh38)
6:27410637 (GRCh37)
Canonical SPDI:: NC_000006.12:27442856:AGA:A
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00017/2 (ALFA)
-=0.00053/36 (GnomAD)
HGVS:: NC_000006.12:g.27442858_27442859del, NC_000006.11:g.27410637_27410638del, NG_052614.1:g.35261_35262del

Select item 149105817917.

rs1491058179 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->AAAAAAAAAAAAAAAAGA
Chromosome:: no mapping
Canonical SPDI:

Select item 149104521518.

rs1491045215 has merged into rs61602778 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:27465030 (GRCh38)
6:27432809 (GRCh37)
Canonical SPDI:: NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:27465016:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.27465030_27465037del, NC_000006.12:g.27465031_27465037del, NC_000006.12:g.27465032_27465037del, NC_000006.12:g.27465033_27465037del, NC_000006.12:g.27465034_27465037del, NC_000006.12:g.27465035_27465037del, NC_000006.12:g.27465036_27465037del, NC_000006.12:g.27465037del, NC_000006.12:g.27465037dup, NC_000006.12:g.27465036_27465037dup, NC_000006.12:g.27465035_27465037dup, NC_000006.12:g.27465034_27465037dup, NC_000006.12:g.27465033_27465037dup, NC_000006.12:g.27465032_27465037dup, NC_000006.12:g.27465031_27465037dup, NC_000006.12:g.27465030_27465037dup, NC_000006.12:g.27465029_27465037dup, NC_000006.12:g.27465028_27465037dup, NC_000006.12:g.27465027_27465037dup, NC_000006.12:g.27465026_27465037dup, NC_000006.12:g.27465025_27465037dup, NC_000006.12:g.27465024_27465037dup, NC_000006.12:g.27465023_27465037dup, NC_000006.12:g.27465022_27465037dup, NC_000006.12:g.27465021_27465037dup, NC_000006.12:g.27465020_27465037dup, NC_000006.12:g.27465019_27465037dup, NC_000006.12:g.27465018_27465037dup, NC_000006.12:g.27465017_27465037dup, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.27465037_27465038insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432809_27432816del, NC_000006.11:g.27432810_27432816del, NC_000006.11:g.27432811_27432816del, NC_000006.11:g.27432812_27432816del, NC_000006.11:g.27432813_27432816del, NC_000006.11:g.27432814_27432816del, NC_000006.11:g.27432815_27432816del, NC_000006.11:g.27432816del, NC_000006.11:g.27432816dup, NC_000006.11:g.27432815_27432816dup, NC_000006.11:g.27432814_27432816dup, NC_000006.11:g.27432813_27432816dup, NC_000006.11:g.27432812_27432816dup, NC_000006.11:g.27432811_27432816dup, NC_000006.11:g.27432810_27432816dup, NC_000006.11:g.27432809_27432816dup, NC_000006.11:g.27432808_27432816dup, NC_000006.11:g.27432807_27432816dup, NC_000006.11:g.27432806_27432816dup, NC_000006.11:g.27432805_27432816dup, NC_000006.11:g.27432804_27432816dup, NC_000006.11:g.27432803_27432816dup, NC_000006.11:g.27432802_27432816dup, NC_000006.11:g.27432801_27432816dup, NC_000006.11:g.27432800_27432816dup, NC_000006.11:g.27432799_27432816dup, NC_000006.11:g.27432798_27432816dup, NC_000006.11:g.27432797_27432816dup, NC_000006.11:g.27432796_27432816dup, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.27432816_27432817insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052614.1:g.13095_13102del, NG_052614.1:g.13096_13102del, NG_052614.1:g.13097_13102del, NG_052614.1:g.13098_13102del, NG_052614.1:g.13099_13102del, NG_052614.1:g.13100_13102del, NG_052614.1:g.13101_13102del, NG_052614.1:g.13102del, NG_052614.1:g.13102dup, NG_052614.1:g.13101_13102dup, NG_052614.1:g.13100_13102dup, NG_052614.1:g.13099_13102dup, NG_052614.1:g.13098_13102dup, NG_052614.1:g.13097_13102dup, NG_052614.1:g.13096_13102dup, NG_052614.1:g.13095_13102dup, NG_052614.1:g.13094_13102dup, NG_052614.1:g.13093_13102dup, NG_052614.1:g.13092_13102dup, NG_052614.1:g.13091_13102dup, NG_052614.1:g.13090_13102dup, NG_052614.1:g.13089_13102dup, NG_052614.1:g.13088_13102dup, NG_052614.1:g.13087_13102dup, NG_052614.1:g.13086_13102dup, NG_052614.1:g.13085_13102dup, NG_052614.1:g.13084_13102dup, NG_052614.1:g.13083_13102dup, NG_052614.1:g.13082_13102dup, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052614.1:g.13102_13103insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149100543019.

rs1491005430 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 6:27465174 (GRCh38)
6:27432953 (GRCh37)
Canonical SPDI:: NC_000006.12:27465172:AGA:A
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.27465174_27465175del, NC_000006.11:g.27432953_27432954del, NG_052614.1:g.12945_12946del

Select item 149097401420.

rs1490974014 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:27463561 (GRCh38)
6:27431340 (GRCh37)
Canonical SPDI:: NC_000006.12:27463560:A:G
Gene:: ZNF184 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.27463561A>G, NC_000006.11:g.27431340A>G, NG_052614.1:g.14558T>C

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