SNP Links for Gene (Select 7407) - SNP

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Select item 14908043771.

rs1490804377 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:31788138 (GRCh38)
6:31755915 (GRCh37)
Canonical SPDI:: NC_000006.12:31788137:T:A,NC_000006.12:31788137:T:C
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.31788138T>A, NC_000006.12:g.31788138T>C, NC_000006.11:g.31755915T>A, NC_000006.11:g.31755915T>C, NG_028229.1:g.12798A>T, NG_028229.1:g.12798A>G, NT_113891.3:g.3265380T>A, NT_113891.3:g.3265380T>C, NT_113891.2:g.3265486T>A, NT_113891.2:g.3265486T>C, NT_167245.2:g.3035912T>A, NT_167245.2:g.3035912T>C, NT_167245.1:g.3041497T>A, NT_167245.1:g.3041497T>C, NT_167247.2:g.3130028T>A, NT_167247.2:g.3130028T>C, NT_167247.1:g.3135613T>A, NT_167247.1:g.3135613T>C, NT_167244.2:g.3120750T>A, NT_167244.2:g.3120750T>C, NT_167244.1:g.3070666T>A, NT_167244.1:g.3070666T>C, NT_167249.2:g.3087430T>A, NT_167249.2:g.3087430T>C, NT_167249.1:g.3086728T>A, NT_167249.1:g.3086728T>C

Select item 14905924242.

rs1490592424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31792184 (GRCh38)
6:31759961 (GRCh37)
Canonical SPDI:: NC_000006.12:31792183:G:A
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000034/9 (TOPMED)
HGVS:: NC_000006.12:g.31792184G>A, NC_000006.11:g.31759961G>A, NG_028229.1:g.8752C>T, NT_113891.3:g.3269424G>A, NT_113891.2:g.3269530G>A, NT_167245.2:g.3039958G>A, NT_167245.1:g.3045543G>A, NT_167247.2:g.3134073G>A, NT_167247.1:g.3139658G>A, NT_167244.2:g.3124795G>A, NT_167244.1:g.3074711G>A, NT_167249.2:g.3091475G>A, NT_167249.1:g.3090773G>A, NT_167248.2:g.3048011G>A, NT_167248.1:g.3053607G>A

Select item 14905894713.

rs1490589471 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31791516 (GRCh38)
6:31759293 (GRCh37)
Canonical SPDI:: NC_000006.12:31791515:A:G
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31791516A>G, NC_000006.11:g.31759293A>G, NG_028229.1:g.9420T>C, NT_113891.3:g.3268756A>G, NT_113891.2:g.3268862A>G, NT_167245.2:g.3039290A>G, NT_167245.1:g.3044875A>G, NT_167247.2:g.3133405A>G, NT_167247.1:g.3138990A>G, NT_167244.2:g.3124127A>G, NT_167244.1:g.3074043A>G, NT_167249.2:g.3090807A>G, NT_167249.1:g.3090105A>G, NT_167248.2:g.3047343A>G, NT_167248.1:g.3052939A>G

Select item 14905741784.

rs1490574178 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31779980 (GRCh38)
6:31747757 (GRCh37)
Canonical SPDI:: NC_000006.12:31779979:C:T
Gene:: VARS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.31779980C>T, NC_000006.11:g.31747757C>T, NG_028229.1:g.20956G>A, NT_113891.3:g.3257222C>T, NT_113891.2:g.3257328C>T, NT_167245.2:g.3027754C>T, NT_167245.1:g.3033339C>T, NT_167247.2:g.3121869C>T, NT_167247.1:g.3127454C>T, NT_167244.2:g.3112591C>T, NT_167244.1:g.3062507C>T, NT_167249.2:g.3079271C>T, NT_167249.1:g.3078569C>T

Select item 14903587245.

rs1490358724 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:31784877 (GRCh38)
6:31752654 (GRCh37)
Canonical SPDI:: NC_000006.12:31784876:G:T
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31784877G>T, NC_000006.11:g.31752654G>T, NG_028229.1:g.16059C>A, NT_113891.3:g.3262120G>T, NT_113891.2:g.3262226G>T, NT_167245.2:g.3032651G>T, NT_167245.1:g.3038236G>T, NT_167247.2:g.3126767G>T, NT_167247.1:g.3132352G>T, NT_167244.2:g.3117489G>T, NT_167244.1:g.3067405G>T, NT_167249.2:g.3084169G>T, NT_167249.1:g.3083467G>T

Select item 14903140926.

rs1490314092 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>G
Chromosome:: no mapping
Canonical SPDI:

Select item 14902610047.

rs1490261004 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31789108 (GRCh38)
6:31756885 (GRCh37)
Canonical SPDI:: NC_000006.12:31789107:A:G
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000043/6 (GnomAD)
HGVS:: NC_000006.12:g.31789108A>G, NC_000006.11:g.31756885A>G, NG_028229.1:g.11828T>C, NT_113891.3:g.3266351A>G, NT_113891.2:g.3266457A>G, NT_167245.2:g.3036882A>G, NT_167245.1:g.3042467A>G, NT_167247.2:g.3130998A>G, NT_167247.1:g.3136583A>G, NT_167244.2:g.3121720A>G, NT_167244.1:g.3071636A>G, NT_167249.2:g.3088400A>G, NT_167249.1:g.3087698A>G, NT_167248.2:g.3044936A>G, NT_167248.1:g.3050532A>G

Select item 14902215408.

rs1490221540 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:31783069 (GRCh38)
6:31750846 (GRCh37)
Canonical SPDI:: NC_000006.12:31783068:T:C
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.31783069T>C, NC_000006.11:g.31750846T>C, NG_028229.1:g.17867A>G, NT_113891.3:g.3260311T>C, NT_113891.2:g.3260417T>C, NT_167245.2:g.3030843T>C, NT_167245.1:g.3036428T>C, NT_167247.2:g.3124958T>C, NT_167247.1:g.3130543T>C, NT_167244.2:g.3115680T>C, NT_167244.1:g.3065596T>C, NT_167249.2:g.3082360T>C, NT_167249.1:g.3081658T>C

Select item 14899856289.

rs1489985628 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31790565 (GRCh38)
6:31758342 (GRCh37)
Canonical SPDI:: NC_000006.12:31790564:G:A
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000009/1 (GnomAD)
HGVS:: NC_000006.12:g.31790565G>A, NC_000006.11:g.31758342G>A, NG_028229.1:g.10371C>T, NT_113891.3:g.3267807G>A, NT_113891.2:g.3267913G>A, NT_167245.2:g.3038339G>A, NT_167245.1:g.3043924G>A, NT_167247.2:g.3132455G>A, NT_167247.1:g.3138040G>A, NT_167244.2:g.3123177G>A, NT_167244.1:g.3073093G>A, NT_167249.2:g.3089857G>A, NT_167249.1:g.3089155G>A, NT_167248.2:g.3046393G>A, NT_167248.1:g.3051989G>A

Select item 148974792210.

rs1489747922 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:31791541 (GRCh38)
6:31759318 (GRCh37)
Canonical SPDI:: NC_000006.12:31791540:G:T
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31791541G>T, NC_000006.11:g.31759318G>T, NG_028229.1:g.9395C>A, NT_113891.3:g.3268781G>T, NT_113891.2:g.3268887G>T, NT_167245.2:g.3039315G>T, NT_167245.1:g.3044900G>T, NT_167247.2:g.3133430G>T, NT_167247.1:g.3139015G>T, NT_167244.2:g.3124152G>T, NT_167244.1:g.3074068G>T, NT_167249.2:g.3090832G>T, NT_167249.1:g.3090130G>T, NT_167248.2:g.3047368G>T, NT_167248.1:g.3052964G>T

Select item 148954012911.

rs1489540129 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31783055 (GRCh38)
6:31750832 (GRCh37)
Canonical SPDI:: NC_000006.12:31783054:C:T
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.31783055C>T, NC_000006.11:g.31750832C>T, NG_028229.1:g.17881G>A, NT_113891.3:g.3260297C>T, NT_113891.2:g.3260403C>T, NT_167245.2:g.3030829C>T, NT_167245.1:g.3036414C>T, NT_167247.2:g.3124944C>T, NT_167247.1:g.3130529C>T, NT_167244.2:g.3115666C>T, NT_167244.1:g.3065582C>T, NT_167249.2:g.3082346C>T, NT_167249.1:g.3081644C>T

Select item 148937656612.

rs1489376566 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 6:31796713 (GRCh38)
6:31764490 (GRCh37)
Canonical SPDI:: NC_000006.12:31796712:C:
Gene:: VARS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.0001/5 (GnomAD)
HGVS:: NC_000006.12:g.31796713del, NC_000006.11:g.31764490del, NG_028229.1:g.4223del, NT_113891.3:g.3273953del, NT_113891.2:g.3274059del, NT_167245.2:g.3044487del, NT_167245.1:g.3050072del, NT_167247.2:g.3138602del, NT_167247.1:g.3144187del, NT_167244.2:g.3129324del, NT_167244.1:g.3079240del, NT_167248.2:g.3052540del, NT_167248.1:g.3058136del

Select item 148922239413.

rs1489222394 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:31778596 (GRCh38)
6:31746373 (GRCh37)
Canonical SPDI:: NC_000006.12:31778595:A:C
Gene:: VARS1 (Varview), VWA7 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.31778596A>C, NC_000006.11:g.31746373A>C, NG_028229.1:g.22340T>G, NT_113891.3:g.3255838A>C, NT_113891.2:g.3255944A>C, NT_167245.2:g.3026370A>C, NT_167245.1:g.3031955A>C, NT_167247.2:g.3120485A>C, NT_167247.1:g.3126070A>C, NT_167244.2:g.3111207A>C, NT_167244.1:g.3061123A>C, NT_167249.2:g.3077887A>C, NT_167249.1:g.3077185A>C

Select item 148918319514.

rs1489183195 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:31795947 (GRCh38)
6:31763724 (GRCh37)
Canonical SPDI:: NC_000006.12:31795946:C:A
Gene:: VARS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.31795947C>A, NC_000006.11:g.31763724C>A, NG_028229.1:g.4989G>T, NT_113891.3:g.3273187C>A, NT_113891.2:g.3273293C>A, NT_167245.2:g.3043721C>A, NT_167245.1:g.3049306C>A, NT_167247.2:g.3137836C>A, NT_167247.1:g.3143421C>A, NT_167244.2:g.3128558C>A, NT_167244.1:g.3078474C>A, NT_167248.2:g.3051774C>A, NT_167248.1:g.3057370C>A

Select item 148872503915.

rs1488725039 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31786220 (GRCh38)
6:31753997 (GRCh37)
Canonical SPDI:: NC_000006.12:31786219:A:G
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31786220A>G, NC_000006.11:g.31753997A>G, NG_028229.1:g.14716T>C, NT_113891.3:g.3263463A>G, NT_113891.2:g.3263569A>G, NT_167245.2:g.3033994A>G, NT_167245.1:g.3039579A>G, NT_167247.2:g.3128110A>G, NT_167247.1:g.3133695A>G, NT_167244.2:g.3118832A>G, NT_167244.1:g.3068748A>G, NT_167249.2:g.3085512A>G, NT_167249.1:g.3084810A>G

Select item 148853804016.

rs1488538040 has merged into rs536213828 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 6:31790115 (GRCh38)
6:31757892 (GRCh37)
Canonical SPDI:: NC_000006.12:31790104:AAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:31790104:AAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:31790104:AAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:31790104:AAAAAAAAAAAA:AAAAAAAAAAAAAA
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0.00007/1 (ALFA)
-=0.2/8 (GENOME_DK)
HGVS:: NC_000006.12:g.31790115_31790116del, NC_000006.12:g.31790116del, NC_000006.12:g.31790116dup, NC_000006.12:g.31790115_31790116dup, NC_000006.11:g.31757892_31757893del, NC_000006.11:g.31757893del, NC_000006.11:g.31757893dup, NC_000006.11:g.31757892_31757893dup, NG_028229.1:g.10830_10831del, NG_028229.1:g.10831del, NG_028229.1:g.10831dup, NG_028229.1:g.10830_10831dup, NT_113891.3:g.3267358dup, NT_113891.3:g.3267358del, NT_113891.3:g.3267357_3267358dup, NT_113891.3:g.3267356_3267358dup, NT_167245.2:g.3037889_3037890del, NT_167245.2:g.3037890del, NT_167245.2:g.3037890dup, NT_167245.2:g.3037889_3037890dup, NT_167245.1:g.3043474_3043475del, NT_167245.1:g.3043475del, NT_167245.1:g.3043475dup, NT_167245.1:g.3043474_3043475dup, NT_167247.2:g.3132005_3132006del, NT_167247.2:g.3132006del, NT_167247.2:g.3132006dup, NT_167247.2:g.3132005_3132006dup, NT_167247.1:g.3137590_3137591del, NT_167247.1:g.3137591del, NT_167247.1:g.3137591dup, NT_167247.1:g.3137590_3137591dup, NT_167244.2:g.3122727_3122728del, NT_167244.2:g.3122728del, NT_167244.2:g.3122728dup, NT_167244.2:g.3122727_3122728dup, NT_167244.1:g.3072643_3072644del, NT_167244.1:g.3072644del, NT_167244.1:g.3072644dup, NT_167244.1:g.3072643_3072644dup, NT_167249.2:g.3089407_3089408del, NT_167249.2:g.3089408del, NT_167249.2:g.3089408dup, NT_167249.2:g.3089407_3089408dup, NT_167249.1:g.3088705_3088706del, NT_167249.1:g.3088706del, NT_167249.1:g.3088706dup, NT_167249.1:g.3088705_3088706dup, NT_167248.2:g.3045943_3045944del, NT_167248.2:g.3045944del, NT_167248.2:g.3045944dup, NT_167248.2:g.3045943_3045944dup, NT_167248.1:g.3051539_3051540del, NT_167248.1:g.3051540del, NT_167248.1:g.3051540dup, NT_167248.1:g.3051539_3051540dup, NT_113891.2:g.3267464dup, NT_113891.2:g.3267464del, NT_113891.2:g.3267463_3267464dup, NT_113891.2:g.3267462_3267464dup

Select item 148820955317.

rs1488209553 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:31789697 (GRCh38)
6:31757474 (GRCh37)
Canonical SPDI:: NC_000006.12:31789696:T:G
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31789697T>G, NC_000006.11:g.31757474T>G, NG_028229.1:g.11239A>C, NT_113891.3:g.3266940T>G, NT_113891.2:g.3267046T>G, NT_167245.2:g.3037471T>G, NT_167245.1:g.3043056T>G, NT_167247.2:g.3131587T>G, NT_167247.1:g.3137172T>G, NT_167244.2:g.3122309T>G, NT_167244.1:g.3072225T>G, NT_167249.2:g.3088989T>G, NT_167249.1:g.3088287T>G, NT_167248.2:g.3045525T>G, NT_167248.1:g.3051121T>G

Select item 148816721818.

rs1488167218 has merged into rs9279419 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:31790611 (GRCh38)
6:31758388 (GRCh37)
Canonical SPDI:: NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:31790602:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: VARS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.31790611_31790631del, NC_000006.12:g.31790613_31790631del, NC_000006.12:g.31790614_31790631del, NC_000006.12:g.31790615_31790631del, NC_000006.12:g.31790616_31790631del, NC_000006.12:g.31790617_31790631del, NC_000006.12:g.31790618_31790631del, NC_000006.12:g.31790619_31790631del, NC_000006.12:g.31790620_31790631del, NC_000006.12:g.31790621_31790631del, NC_000006.12:g.31790622_31790631del, NC_000006.12:g.31790623_31790631del, NC_000006.12:g.31790624_31790631del, NC_000006.12:g.31790625_31790631del, NC_000006.12:g.31790626_31790631del, NC_000006.12:g.31790627_31790631del, NC_000006.12:g.31790628_31790631del, NC_000006.12:g.31790629_31790631del, NC_000006.12:g.31790630_31790631del, NC_000006.12:g.31790631del, NC_000006.12:g.31790631dup, NC_000006.12:g.31790630_31790631dup, NC_000006.12:g.31790629_31790631dup, NC_000006.12:g.31790628_31790631dup, NC_000006.12:g.31790627_31790631dup, NC_000006.12:g.31790626_31790631dup, NC_000006.12:g.31790625_31790631dup, NC_000006.12:g.31790624_31790631dup, NC_000006.12:g.31790623_31790631dup, NC_000006.12:g.31790621_31790631dup, NC_000006.12:g.31790620_31790631dup, NC_000006.12:g.31790617_31790631dup, NC_000006.12:g.31790605_31790631dup, NC_000006.12:g.31790631_31790632insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.31758388_31758408del, NC_000006.11:g.31758390_31758408del, NC_000006.11:g.31758391_31758408del, NC_000006.11:g.31758392_31758408del, NC_000006.11:g.31758393_31758408del, NC_000006.11:g.31758394_31758408del, NC_000006.11:g.31758395_31758408del, NC_000006.11:g.31758396_31758408del, NC_000006.11:g.31758397_31758408del, NC_000006.11:g.31758398_31758408del, NC_000006.11:g.31758399_31758408del, NC_000006.11:g.31758400_31758408del, NC_000006.11:g.31758401_31758408del, NC_000006.11:g.31758402_31758408del, NC_000006.11:g.31758403_31758408del, NC_000006.11:g.31758404_31758408del, NC_000006.11:g.31758405_31758408del, NC_000006.11:g.31758406_31758408del, NC_000006.11:g.31758407_31758408del, NC_000006.11:g.31758408del, NC_000006.11:g.31758408dup, NC_000006.11:g.31758407_31758408dup, NC_000006.11:g.31758406_31758408dup, NC_000006.11:g.31758405_31758408dup, NC_000006.11:g.31758404_31758408dup, NC_000006.11:g.31758403_31758408dup, NC_000006.11:g.31758402_31758408dup, NC_000006.11:g.31758401_31758408dup, NC_000006.11:g.31758400_31758408dup, NC_000006.11:g.31758398_31758408dup, NC_000006.11:g.31758397_31758408dup, NC_000006.11:g.31758394_31758408dup, NC_000006.11:g.31758382_31758408dup, NC_000006.11:g.31758408_31758409insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028229.1:g.10313_10333del, NG_028229.1:g.10315_10333del, NG_028229.1:g.10316_10333del, NG_028229.1:g.10317_10333del, NG_028229.1:g.10318_10333del, NG_028229.1:g.10319_10333del, NG_028229.1:g.10320_10333del, NG_028229.1:g.10321_10333del, NG_028229.1:g.10322_10333del, NG_028229.1:g.10323_10333del, NG_028229.1:g.10324_10333del, NG_028229.1:g.10325_10333del, NG_028229.1:g.10326_10333del, NG_028229.1:g.10327_10333del, NG_028229.1:g.10328_10333del, NG_028229.1:g.10329_10333del, NG_028229.1:g.10330_10333del, NG_028229.1:g.10331_10333del, NG_028229.1:g.10332_10333del, NG_028229.1:g.10333del, NG_028229.1:g.10333dup, NG_028229.1:g.10332_10333dup, NG_028229.1:g.10331_10333dup, NG_028229.1:g.10330_10333dup, NG_028229.1:g.10329_10333dup, NG_028229.1:g.10328_10333dup, NG_028229.1:g.10327_10333dup, NG_028229.1:g.10326_10333dup, NG_028229.1:g.10325_10333dup, NG_028229.1:g.10323_10333dup, NG_028229.1:g.10322_10333dup, NG_028229.1:g.10319_10333dup, NG_028229.1:g.10307_10333dup, NG_028229.1:g.10333_10334insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.3267870_3267871dup, NT_113891.3:g.3267853_3267871del, NT_113891.3:g.3267855_3267871del, NT_113891.3:g.3267856_3267871del, NT_113891.3:g.3267857_3267871del, NT_113891.3:g.3267858_3267871del, NT_113891.3:g.3267859_3267871del, NT_113891.3:g.3267860_3267871del, NT_113891.3:g.3267861_3267871del, NT_113891.3:g.3267862_3267871del, NT_113891.3:g.3267863_3267871del, NT_113891.3:g.3267864_3267871del, NT_113891.3:g.3267865_3267871del, NT_113891.3:g.3267866_3267871del, NT_113891.3:g.3267867_3267871del, NT_113891.3:g.3267868_3267871del, NT_113891.3:g.3267869_3267871del, NT_113891.3:g.3267870_3267871del, NT_113891.3:g.3267871del, NT_113891.3:g.3267871dup, NT_113891.3:g.3267869_3267871dup, NT_113891.3:g.3267868_3267871dup, NT_113891.3:g.3267867_3267871dup, NT_113891.3:g.3267866_3267871dup, NT_113891.3:g.3267865_3267871dup, NT_113891.3:g.3267864_3267871dup, NT_113891.3:g.3267863_3267871dup, NT_113891.3:g.3267862_3267871dup, NT_113891.3:g.3267861_3267871dup, NT_113891.3:g.3267859_3267871dup, NT_113891.3:g.3267858_3267871dup, NT_113891.3:g.3267855_3267871dup, NT_113891.3:g.3267871_3267872insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3267871_3267872insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3038385_3038405del, NT_167245.2:g.3038387_3038405del, NT_167245.2:g.3038388_3038405del, NT_167245.2:g.3038389_3038405del, NT_167245.2:g.3038390_3038405del, NT_167245.2:g.3038391_3038405del, NT_167245.2:g.3038392_3038405del, NT_167245.2:g.3038393_3038405del, NT_167245.2:g.3038394_3038405del, NT_167245.2:g.3038395_3038405del, NT_167245.2:g.3038396_3038405del, NT_167245.2:g.3038397_3038405del, NT_167245.2:g.3038398_3038405del, NT_167245.2:g.3038399_3038405del, NT_167245.2:g.3038400_3038405del, NT_167245.2:g.3038401_3038405del, NT_167245.2:g.3038402_3038405del, NT_167245.2:g.3038403_3038405del, NT_167245.2:g.3038404_3038405del, NT_167245.2:g.3038405del, NT_167245.2:g.3038405dup, NT_167245.2:g.3038404_3038405dup, NT_167245.2:g.3038403_3038405dup, NT_167245.2:g.3038402_3038405dup, NT_167245.2:g.3038401_3038405dup, NT_167245.2:g.3038400_3038405dup, NT_167245.2:g.3038399_3038405dup, NT_167245.2:g.3038398_3038405dup, NT_167245.2:g.3038397_3038405dup, NT_167245.2:g.3038395_3038405dup, NT_167245.2:g.3038394_3038405dup, NT_167245.2:g.3038391_3038405dup, NT_167245.2:g.3038379_3038405dup, NT_167245.2:g.3038405_3038406insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3043970_3043990del, NT_167245.1:g.3043972_3043990del, NT_167245.1:g.3043973_3043990del, NT_167245.1:g.3043974_3043990del, NT_167245.1:g.3043975_3043990del, NT_167245.1:g.3043976_3043990del, NT_167245.1:g.3043977_3043990del, NT_167245.1:g.3043978_3043990del, NT_167245.1:g.3043979_3043990del, NT_167245.1:g.3043980_3043990del, NT_167245.1:g.3043981_3043990del, NT_167245.1:g.3043982_3043990del, NT_167245.1:g.3043983_3043990del, NT_167245.1:g.3043984_3043990del, NT_167245.1:g.3043985_3043990del, NT_167245.1:g.3043986_3043990del, NT_167245.1:g.3043987_3043990del, NT_167245.1:g.3043988_3043990del, NT_167245.1:g.3043989_3043990del, NT_167245.1:g.3043990del, NT_167245.1:g.3043990dup, NT_167245.1:g.3043989_3043990dup, NT_167245.1:g.3043988_3043990dup, NT_167245.1:g.3043987_3043990dup, NT_167245.1:g.3043986_3043990dup, NT_167245.1:g.3043985_3043990dup, NT_167245.1:g.3043984_3043990dup, NT_167245.1:g.3043983_3043990dup, NT_167245.1:g.3043982_3043990dup, NT_167245.1:g.3043980_3043990dup, NT_167245.1:g.3043979_3043990dup, NT_167245.1:g.3043976_3043990dup, NT_167245.1:g.3043964_3043990dup, NT_167245.1:g.3043990_3043991insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3132520dup, NT_167247.2:g.3132501_3132520del, NT_167247.2:g.3132503_3132520del, NT_167247.2:g.3132504_3132520del, NT_167247.2:g.3132505_3132520del, NT_167247.2:g.3132506_3132520del, NT_167247.2:g.3132507_3132520del, NT_167247.2:g.3132508_3132520del, NT_167247.2:g.3132509_3132520del, NT_167247.2:g.3132510_3132520del, NT_167247.2:g.3132511_3132520del, NT_167247.2:g.3132512_3132520del, NT_167247.2:g.3132513_3132520del, NT_167247.2:g.3132514_3132520del, NT_167247.2:g.3132515_3132520del, NT_167247.2:g.3132516_3132520del, NT_167247.2:g.3132517_3132520del, NT_167247.2:g.3132518_3132520del, NT_167247.2:g.3132519_3132520del, NT_167247.2:g.3132520del, NT_167247.2:g.3132519_3132520dup, NT_167247.2:g.3132518_3132520dup, NT_167247.2:g.3132517_3132520dup, NT_167247.2:g.3132516_3132520dup, NT_167247.2:g.3132515_3132520dup, NT_167247.2:g.3132514_3132520dup, NT_167247.2:g.3132513_3132520dup, NT_167247.2:g.3132512_3132520dup, NT_167247.2:g.3132511_3132520dup, NT_167247.2:g.3132509_3132520dup, NT_167247.2:g.3132508_3132520dup, NT_167247.2:g.3132505_3132520dup, NT_167247.2:g.3132493_3132520dup, NT_167247.2:g.3132520_3132521insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3123242dup, NT_167244.2:g.3123223_3123242del, NT_167244.2:g.3123225_3123242del, NT_167244.2:g.3123226_3123242del, NT_167244.2:g.3123227_3123242del, NT_167244.2:g.3123228_3123242del, NT_167244.2:g.3123229_3123242del, NT_167244.2:g.3123230_3123242del, NT_167244.2:g.3123231_3123242del, NT_167244.2:g.3123232_3123242del, NT_167244.2:g.3123233_3123242del, NT_167244.2:g.3123234_3123242del, NT_167244.2:g.3123235_3123242del, NT_167244.2:g.3123236_3123242del, NT_167244.2:g.3123237_3123242del, NT_167244.2:g.3123238_3123242del, NT_167244.2:g.3123239_3123242del, NT_167244.2:g.3123240_3123242del, NT_167244.2:g.3123241_3123242del, NT_167244.2:g.3123242del, NT_167244.2:g.3123241_3123242dup, NT_167244.2:g.3123240_3123242dup, NT_167244.2:g.3123239_3123242dup, NT_167244.2:g.3123238_3123242dup, NT_167244.2:g.3123237_3123242dup, NT_167244.2:g.3123236_3123242dup, NT_167244.2:g.3123235_3123242dup, NT_167244.2:g.3123234_3123242dup, NT_167244.2:g.3123233_3123242dup, NT_167244.2:g.3123231_3123242dup, NT_167244.2:g.3123230_3123242dup, NT_167244.2:g.3123227_3123242dup, NT_167244.2:g.3123215_3123242dup, NT_167244.2:g.3123242_3123243insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3089922dup, NT_167249.2:g.3089903_3089922del, NT_167249.2:g.3089905_3089922del, NT_167249.2:g.3089906_3089922del, NT_167249.2:g.3089907_3089922del, NT_167249.2:g.3089908_3089922del, NT_167249.2:g.3089909_3089922del, NT_167249.2:g.3089910_3089922del, NT_167249.2:g.3089911_3089922del, NT_167249.2:g.3089912_3089922del, NT_167249.2:g.3089913_3089922del, NT_167249.2:g.3089914_3089922del, NT_167249.2:g.3089915_3089922del, NT_167249.2:g.3089916_3089922del, NT_167249.2:g.3089917_3089922del, NT_167249.2:g.3089918_3089922del, NT_167249.2:g.3089919_3089922del, NT_167249.2:g.3089920_3089922del, NT_167249.2:g.3089921_3089922del, NT_167249.2:g.3089922del, NT_167249.2:g.3089921_3089922dup, NT_167249.2:g.3089920_3089922dup, NT_167249.2:g.3089919_3089922dup, NT_167249.2:g.3089918_3089922dup, NT_167249.2:g.3089917_3089922dup, NT_167249.2:g.3089916_3089922dup, NT_167249.2:g.3089915_3089922dup, NT_167249.2:g.3089914_3089922dup, NT_167249.2:g.3089913_3089922dup, NT_167249.2:g.3089911_3089922dup, NT_167249.2:g.3089910_3089922dup, NT_167249.2:g.3089907_3089922dup, NT_167249.2:g.3089895_3089922dup, NT_167249.2:g.3089922_3089923insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3046458dup, NT_167248.2:g.3046439_3046458del, NT_167248.2:g.3046441_3046458del, NT_167248.2:g.3046442_3046458del, NT_167248.2:g.3046443_3046458del, NT_167248.2:g.3046444_3046458del, NT_167248.2:g.3046445_3046458del, NT_167248.2:g.3046446_3046458del, NT_167248.2:g.3046447_3046458del, NT_167248.2:g.3046448_3046458del, NT_167248.2:g.3046449_3046458del, NT_167248.2:g.3046450_3046458del, NT_167248.2:g.3046451_3046458del, NT_167248.2:g.3046452_3046458del, NT_167248.2:g.3046453_3046458del, NT_167248.2:g.3046454_3046458del, NT_167248.2:g.3046455_3046458del, NT_167248.2:g.3046456_3046458del, NT_167248.2:g.3046457_3046458del, NT_167248.2:g.3046458del, NT_167248.2:g.3046457_3046458dup, NT_167248.2:g.3046456_3046458dup, NT_167248.2:g.3046455_3046458dup, NT_167248.2:g.3046454_3046458dup, NT_167248.2:g.3046453_3046458dup, NT_167248.2:g.3046452_3046458dup, NT_167248.2:g.3046451_3046458dup, NT_167248.2:g.3046450_3046458dup, NT_167248.2:g.3046449_3046458dup, NT_167248.2:g.3046447_3046458dup, NT_167248.2:g.3046446_3046458dup, NT_167248.2:g.3046443_3046458dup, NT_167248.2:g.3046431_3046458dup, NT_167248.2:g.3046458_3046459insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3267976_3267977dup, NT_113891.2:g.3267959_3267977del, NT_113891.2:g.3267961_3267977del, NT_113891.2:g.3267962_3267977del, NT_113891.2:g.3267963_3267977del, NT_113891.2:g.3267964_3267977del, NT_113891.2:g.3267965_3267977del, NT_113891.2:g.3267966_3267977del, NT_113891.2:g.3267967_3267977del, NT_113891.2:g.3267968_3267977del, NT_113891.2:g.3267969_3267977del, NT_113891.2:g.3267970_3267977del, NT_113891.2:g.3267971_3267977del, NT_113891.2:g.3267972_3267977del, NT_113891.2:g.3267973_3267977del, NT_113891.2:g.3267974_3267977del, NT_113891.2:g.3267975_3267977del, NT_113891.2:g.3267976_3267977del, NT_113891.2:g.3267977del, NT_113891.2:g.3267977dup, NT_113891.2:g.3267975_3267977dup, NT_113891.2:g.3267974_3267977dup, NT_113891.2:g.3267973_3267977dup, NT_113891.2:g.3267972_3267977dup, NT_113891.2:g.3267971_3267977dup, NT_113891.2:g.3267970_3267977dup, NT_113891.2:g.3267969_3267977dup, NT_113891.2:g.3267968_3267977dup, NT_113891.2:g.3267967_3267977dup, NT_113891.2:g.3267965_3267977dup, NT_113891.2:g.3267964_3267977dup, NT_113891.2:g.3267961_3267977dup, NT_113891.2:g.3267977_3267978insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3267977_3267978insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3052054dup, NT_167248.1:g.3052035_3052054del, NT_167248.1:g.3052037_3052054del, NT_167248.1:g.3052038_3052054del, NT_167248.1:g.3052039_3052054del, NT_167248.1:g.3052040_3052054del, NT_167248.1:g.3052041_3052054del, NT_167248.1:g.3052042_3052054del, NT_167248.1:g.3052043_3052054del, NT_167248.1:g.3052044_3052054del, NT_167248.1:g.3052045_3052054del, NT_167248.1:g.3052046_3052054del, NT_167248.1:g.3052047_3052054del, NT_167248.1:g.3052048_3052054del, NT_167248.1:g.3052049_3052054del, NT_167248.1:g.3052050_3052054del, NT_167248.1:g.3052051_3052054del, NT_167248.1:g.3052052_3052054del, NT_167248.1:g.3052053_3052054del, NT_167248.1:g.3052054del, NT_167248.1:g.3052053_3052054dup, NT_167248.1:g.3052052_3052054dup, NT_167248.1:g.3052051_3052054dup, NT_167248.1:g.3052050_3052054dup, NT_167248.1:g.3052049_3052054dup, NT_167248.1:g.3052048_3052054dup, NT_167248.1:g.3052047_3052054dup, NT_167248.1:g.3052046_3052054dup, NT_167248.1:g.3052045_3052054dup, NT_167248.1:g.3052043_3052054dup, NT_167248.1:g.3052042_3052054dup, NT_167248.1:g.3052039_3052054dup, NT_167248.1:g.3052027_3052054dup, NT_167248.1:g.3052054_3052055insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3089220dup, NT_167249.1:g.3089201_3089220del, NT_167249.1:g.3089203_3089220del, NT_167249.1:g.3089204_3089220del, NT_167249.1:g.3089205_3089220del, NT_167249.1:g.3089206_3089220del, NT_167249.1:g.3089207_3089220del, NT_167249.1:g.3089208_3089220del, NT_167249.1:g.3089209_3089220del, NT_167249.1:g.3089210_3089220del, NT_167249.1:g.3089211_3089220del, NT_167249.1:g.3089212_3089220del, NT_167249.1:g.3089213_3089220del, NT_167249.1:g.3089214_3089220del, NT_167249.1:g.3089215_3089220del, NT_167249.1:g.3089216_3089220del, NT_167249.1:g.3089217_3089220del, NT_167249.1:g.3089218_3089220del, NT_167249.1:g.3089219_3089220del, NT_167249.1:g.3089220del, NT_167249.1:g.3089219_3089220dup, NT_167249.1:g.3089218_3089220dup, NT_167249.1:g.3089217_3089220dup, NT_167249.1:g.3089216_3089220dup, NT_167249.1:g.3089215_3089220dup, NT_167249.1:g.3089214_3089220dup, NT_167249.1:g.3089213_3089220dup, NT_167249.1:g.3089212_3089220dup, NT_167249.1:g.3089211_3089220dup, NT_167249.1:g.3089209_3089220dup, NT_167249.1:g.3089208_3089220dup, NT_167249.1:g.3089205_3089220dup, NT_167249.1:g.3089193_3089220dup, NT_167249.1:g.3089220_3089221insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3138105dup, NT_167247.1:g.3138086_3138105del, NT_167247.1:g.3138088_3138105del, NT_167247.1:g.3138089_3138105del, NT_167247.1:g.3138090_3138105del, NT_167247.1:g.3138091_3138105del, NT_167247.1:g.3138092_3138105del, NT_167247.1:g.3138093_3138105del, NT_167247.1:g.3138094_3138105del, NT_167247.1:g.3138095_3138105del, NT_167247.1:g.3138096_3138105del, NT_167247.1:g.3138097_3138105del, NT_167247.1:g.3138098_3138105del, NT_167247.1:g.3138099_3138105del, NT_167247.1:g.3138100_3138105del, NT_167247.1:g.3138101_3138105del, NT_167247.1:g.3138102_3138105del, NT_167247.1:g.3138103_3138105del, NT_167247.1:g.3138104_3138105del, NT_167247.1:g.3138105del, NT_167247.1:g.3138104_3138105dup, NT_167247.1:g.3138103_3138105dup, NT_167247.1:g.3138102_3138105dup, NT_167247.1:g.3138101_3138105dup, NT_167247.1:g.3138100_3138105dup, NT_167247.1:g.3138099_3138105dup, NT_167247.1:g.3138098_3138105dup, NT_167247.1:g.3138097_3138105dup, NT_167247.1:g.3138096_3138105dup, NT_167247.1:g.3138094_3138105dup, NT_167247.1:g.3138093_3138105dup, NT_167247.1:g.3138090_3138105dup, NT_167247.1:g.3138078_3138105dup, NT_167247.1:g.3138105_3138106insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3073158dup, NT_167244.1:g.3073139_3073158del, NT_167244.1:g.3073141_3073158del, NT_167244.1:g.3073142_3073158del, NT_167244.1:g.3073143_3073158del, NT_167244.1:g.3073144_3073158del, NT_167244.1:g.3073145_3073158del, NT_167244.1:g.3073146_3073158del, NT_167244.1:g.3073147_3073158del, NT_167244.1:g.3073148_3073158del, NT_167244.1:g.3073149_3073158del, NT_167244.1:g.3073150_3073158del, NT_167244.1:g.3073151_3073158del, NT_167244.1:g.3073152_3073158del, NT_167244.1:g.3073153_3073158del, NT_167244.1:g.3073154_3073158del, NT_167244.1:g.3073155_3073158del, NT_167244.1:g.3073156_3073158del, NT_167244.1:g.3073157_3073158del, NT_167244.1:g.3073158del, NT_167244.1:g.3073157_3073158dup, NT_167244.1:g.3073156_3073158dup, NT_167244.1:g.3073155_3073158dup, NT_167244.1:g.3073154_3073158dup, NT_167244.1:g.3073153_3073158dup, NT_167244.1:g.3073152_3073158dup, NT_167244.1:g.3073151_3073158dup, NT_167244.1:g.3073150_3073158dup, NT_167244.1:g.3073149_3073158dup, NT_167244.1:g.3073147_3073158dup, NT_167244.1:g.3073146_3073158dup, NT_167244.1:g.3073143_3073158dup, NT_167244.1:g.3073131_3073158dup, NT_167244.1:g.3073158_3073159insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 148705945719.

rs1487059457 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>A
Chromosome:: no mapping
Canonical SPDI:

Select item 148676933520.

rs1486769335 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:31796117 (GRCh38)
6:31763894 (GRCh37)
Canonical SPDI:: NC_000006.12:31796116:G:C
Gene:: VARS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.31796117G>C, NC_000006.11:g.31763894G>C, NG_028229.1:g.4819C>G, NT_113891.3:g.3273357G>C, NT_113891.2:g.3273463G>C, NT_167245.2:g.3043891G>C, NT_167245.1:g.3049476G>C, NT_167247.2:g.3138006G>C, NT_167247.1:g.3143591G>C, NT_167244.2:g.3128728G>C, NT_167244.1:g.3078644G>C, NT_167248.2:g.3051944G>C, NT_167248.1:g.3057540G>C

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