SNP Links for Nucleotide (Select 262205681) - SNP

Select item 14804731451.

rs1480473145 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13836352 (GRCh38)
19:13947166 (GRCh37)
Canonical SPDI:: NC_000019.10:13836351:A:G
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836352A>G, NC_000019.9:g.13947166A>G, NW_021160022.1:g.48193A>G, NR_036515.2:n.6567T>C, NR_029497.1:n.8T>C

Select item 14492438812.

rs1449243881 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13836308 (GRCh38)
19:13947122 (GRCh37)
Canonical SPDI:: NC_000019.10:13836307:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,non_coding_transcript_variant
HGVS:: NC_000019.10:g.13836308C>T, NC_000019.9:g.13947122C>T, NW_021160022.1:g.48149C>T, NR_036515.2:n.6611G>A, NR_029497.1:n.52G>A

Select item 14011874843.

rs1401187484 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13836295 (GRCh38)
19:13947109 (GRCh37)
Canonical SPDI:: NC_000019.10:13836294:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,non_coding_transcript_variant,500B_downstream_variant
HGVS:: NC_000019.10:g.13836295C>T, NC_000019.9:g.13947109C>T, NW_021160022.1:g.48136C>T, NR_036515.2:n.6624G>A, NR_029497.1:n.65G>A

Select item 14004026804.

rs1400402680 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:13836315 (GRCh38)
19:13947129 (GRCh37)
Canonical SPDI:: NC_000019.10:13836314:A:C
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,non_coding_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.13836315A>C, NC_000019.9:g.13947129A>C, NW_021160022.1:g.48156A>C, NR_036515.2:n.6604T>G, NR_029497.1:n.45T>G

Select item 13723316835.

rs1372331683 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:13836312 (GRCh38)
19:13947126 (GRCh37)
Canonical SPDI:: NC_000019.10:13836311:T:C
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency
MAF:: C=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836312T>C, NC_000019.9:g.13947126T>C, NW_021160022.1:g.48153T>C, NR_036515.2:n.6607A>G, NR_029497.1:n.48A>G

Select item 13325224186.

rs1332522418 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13836325 (GRCh38)
19:13947139 (GRCh37)
Canonical SPDI:: NC_000019.10:13836324:A:G
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.13836325A>G, NC_000019.9:g.13947139A>G, NW_021160022.1:g.48166A>G, NR_036515.2:n.6594T>C, NR_029497.1:n.35T>C

Select item 13213617667.

rs1321361766 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13836326 (GRCh38)
19:13947140 (GRCh37)
Canonical SPDI:: NC_000019.10:13836325:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,non_coding_transcript_variant,500B_downstream_variant
HGVS:: NC_000019.10:g.13836326C>T, NC_000019.9:g.13947140C>T, NW_021160022.1:g.48167C>T, NR_036515.2:n.6593G>A, NR_029497.1:n.34G>A

Select item 12967364958.

rs1296736495 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13836310 (GRCh38)
19:13947124 (GRCh37)
Canonical SPDI:: NC_000019.10:13836309:A:G
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,non_coding_transcript_variant,500B_downstream_variant
HGVS:: NC_000019.10:g.13836310A>G, NC_000019.9:g.13947124A>G, NW_021160022.1:g.48151A>G, NR_036515.2:n.6609T>C, NR_029497.1:n.50T>C

Select item 12581155739.

rs1258115573 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:13836344 (GRCh38)
19:13947158 (GRCh37)
Canonical SPDI:: NC_000019.10:13836343:G:A
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: 500B_downstream_variant,non_coding_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836344G>A, NC_000019.9:g.13947158G>A, NW_021160022.1:g.48185G>A, NR_036515.2:n.6575C>T, NR_029497.1:n.16C>T

Select item 122231927810.

rs1222319278 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:13836329 (GRCh38)
19:13947143 (GRCh37)
Canonical SPDI:: NC_000019.10:13836328:T:A
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836329T>A, NC_000019.9:g.13947143T>A, NW_021160022.1:g.48170T>A, NR_036515.2:n.6590A>T, NR_029497.1:n.31A>T

Select item 120199961611.

rs1201999616 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:13836348 (GRCh38)
19:13947162 (GRCh37)
Canonical SPDI:: NC_000019.10:13836347:C:G,NC_000019.10:13836347:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000051/1 (ALFA)
G=0./0 (GnomAD)
HGVS:: NC_000019.10:g.13836348C>G, NC_000019.10:g.13836348C>T, NC_000019.9:g.13947162C>G, NC_000019.9:g.13947162C>T, NW_021160022.1:g.48189C>G, NW_021160022.1:g.48189C>T, NR_036515.2:n.6571G>C, NR_036515.2:n.6571G>A, NR_029497.1:n.12G>C, NR_029497.1:n.12G>A

Select item 117582769412.

rs1175827694 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 19:13836289 (GRCh38)
19:13947103 (GRCh37)
Canonical SPDI:: NC_000019.10:13836288:CT:
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency
MAF:: -=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836289_13836290del, NC_000019.9:g.13947103_13947104del, NW_021160022.1:g.48130_48131del, NR_036515.2:n.6629_6630del, NR_036515.1:n.0_1insA, NR_036515.1:n.4del, NR_029497.1:n.70_71del

Select item 76591876513.

rs765918765 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:13836323 (GRCh38)
19:13947137 (GRCh37)
Canonical SPDI:: NC_000019.10:13836322:C:A
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0./0 (ExAC)
HGVS:: NC_000019.10:g.13836323C>A, NC_000019.9:g.13947137C>A, NW_021160022.1:g.48164C>A, NR_036515.2:n.6596G>T, NR_029497.1:n.37G>T

Select item 75552917914.

rs755529179 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13836316 (GRCh38)
19:13947130 (GRCh37)
Canonical SPDI:: NC_000019.10:13836315:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000044/8 (GnomAD_exomes)
T=0.00008/2 (ExAC)
HGVS:: NC_000019.10:g.13836316C>T, NC_000019.9:g.13947130C>T, NW_021160022.1:g.48157C>T, NR_036515.2:n.6603G>A, NR_029497.1:n.44G>A

Select item 75473715115.

rs754737151 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:13836349 (GRCh38)
19:13947163 (GRCh37)
Canonical SPDI:: NC_000019.10:13836348:G:A
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000031/6 (GnomAD_exomes)
A=0.000043/6 (GnomAD)
A=0.000053/14 (TOPMED)
A=0.000126/4 (ExAC)
HGVS:: NC_000019.10:g.13836349G>A, NC_000019.9:g.13947163G>A, NW_021160022.1:g.48190G>A, NR_036515.2:n.6570C>T, NR_029497.1:n.11C>T

Select item 54949013016.

rs549490130 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13836356 (GRCh38)
19:13947170 (GRCh37)
Canonical SPDI:: NC_000019.10:13836355:A:G
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000019/5 (TOPMED)
G=0.00002/4 (GnomAD_exomes)
G=0.000058/2 (ExAC)
G=0.000312/2 (1000Genomes)
HGVS:: NC_000019.10:g.13836356A>G, NC_000019.9:g.13947170A>G, NW_021160022.1:g.48197A>G, NR_036515.2:n.6563T>C, NR_029497.1:n.4T>C

Select item 36927061017.

rs369270610 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:13836345 (GRCh38)
19:13947159 (GRCh37)
Canonical SPDI:: NC_000019.10:13836344:G:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (ExAC)
T=0.000014/2 (GnomAD)
T=0.000026/7 (TOPMED)
T=0.000097/1 (GoESP)
HGVS:: NC_000019.10:g.13836345G>T, NC_000019.9:g.13947159G>T, NW_021160022.1:g.48186G>T, NR_036515.2:n.6574C>A, NR_029497.1:n.15C>A

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