SNP Links for Gene (Select 284454) - SNP

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Select item 14904330271.

rs1490433027 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13837333 (GRCh38)
19:13948147 (GRCh37)
Canonical SPDI:: NC_000019.10:13837332:A:G
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_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_000019.10:g.13837333A>G, NC_000019.9:g.13948147A>G, NW_021160022.1:g.49174A>G, NR_036515.2:n.5586T>C

Select item 14903023302.

rs1490302330 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 19:13837430 (GRCh38)
19:13948244 (GRCh37)
Canonical SPDI:: NC_000019.10:13837429:G:A,NC_000019.10:13837429:G:C,NC_000019.10:13837429:G:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00004/1 (TOMMO)
HGVS:: NC_000019.10:g.13837430G>A, NC_000019.10:g.13837430G>C, NC_000019.10:g.13837430G>T, NC_000019.9:g.13948244G>A, NC_000019.9:g.13948244G>C, NC_000019.9:g.13948244G>T, NW_021160022.1:g.49271G>A, NW_021160022.1:g.49271G>C, NW_021160022.1:g.49271G>T, NR_036515.2:n.5489C>T, NR_036515.2:n.5489C>G, NR_036515.2:n.5489C>A

Select item 14899820783.

rs1489982078 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:13836426 (GRCh38)
19:13947240 (GRCh37)
Canonical SPDI:: NC_000019.10:13836425:G:A,NC_000019.10:13836425:G:C
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,downstream_transcript_variant,upstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
C=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836426G>A, NC_000019.10:g.13836426G>C, NC_000019.9:g.13947240G>A, NC_000019.9:g.13947240G>C, NW_021160022.1:g.48267G>A, NW_021160022.1:g.48267G>C, NR_036515.2:n.6493C>T, NR_036515.2:n.6493C>G

Select item 14884953954.

rs1488495395 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13835713 (GRCh38)
19:13946527 (GRCh37)
Canonical SPDI:: NC_000019.10:13835712:C:T
Gene:: MIR23AHG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.13835713C>T, NC_000019.9:g.13946527C>T, NW_021160022.1:g.47554C>T, NR_036515.2:n.7206G>A, NR_036515.1:n.577G>A

Select item 14874801405.

rs1487480140 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:13837070 (GRCh38)
19:13947884 (GRCh37)
Canonical SPDI:: NC_000019.10:13837069:G:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.13837070G>T, NC_000019.9:g.13947884G>T, NW_021160022.1:g.48911G>T, NR_036515.2:n.5849C>A

Select item 14865683956.

rs1486568395 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13834035 (GRCh38)
19:13944849 (GRCh37)
Canonical SPDI:: NC_000019.10:13834034:C:T
Gene:: MIR23AHG (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.13834035C>T, NC_000019.9:g.13944849C>T, NW_021160022.1:g.45876C>T

Select item 14856192567.

rs1485619256 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:13835560 (GRCh38)
19:13946374 (GRCh37)
Canonical SPDI:: NC_000019.10:13835559:G:T
Gene:: MIR23AHG (Varview)
Functional Consequence:: non_coding_transcript_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_000019.10:g.13835560G>T, NC_000019.9:g.13946374G>T, NW_021160022.1:g.47401G>T, NR_036515.2:n.7359C>A, NR_036515.1:n.730C>A

Select item 14851936228.

rs1485193622 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 19:13834632 (GRCh38)
19:13945446 (GRCh37)
Canonical SPDI:: NC_000019.10:13834631:A:G,NC_000019.10:13834631:A:T
Gene:: MIR23AHG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.13834632A>G, NC_000019.10:g.13834632A>T, NC_000019.9:g.13945446A>G, NC_000019.9:g.13945446A>T, NW_021160022.1:g.46473A>G, NW_021160022.1:g.46473A>T, NR_036515.2:n.8287T>C, NR_036515.2:n.8287T>A, NR_036515.1:n.1658T>C, NR_036515.1:n.1658T>A

Select item 14845697919.

rs1484569791 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:13835918 (GRCh38)
19:13946732 (GRCh37)
Canonical SPDI:: NC_000019.10:13835917:G:A
Gene:: MIR23AHG (Varview), MIR24-2 (Varview)
Functional Consequence:: non_coding_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.13835918G>A, NC_000019.9:g.13946732G>A, NW_021160022.1:g.47759G>A, NR_036515.2:n.7001C>T, NR_036515.1:n.372C>T

Select item 148453866910.

rs1484538669 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13835843 (GRCh38)
19:13946657 (GRCh37)
Canonical SPDI:: NC_000019.10:13835842:A:G
Gene:: MIR23AHG (Varview), MIR24-2 (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=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.13835843A>G, NC_000019.9:g.13946657A>G, NW_021160022.1:g.47684A>G, NR_036515.2:n.7076T>C, NR_036515.1:n.447T>C

Select item 148331502111.

rs1483315021 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:13836729 (GRCh38)
19:13947543 (GRCh37)
Canonical SPDI:: NC_000019.10:13836728:G:A,NC_000019.10:13836728:G:C
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.13836729G>A, NC_000019.10:g.13836729G>C, NC_000019.9:g.13947543G>A, NC_000019.9:g.13947543G>C, NW_021160022.1:g.48570G>A, NW_021160022.1:g.48570G>C, NR_036515.2:n.6190C>T, NR_036515.2:n.6190C>G

Select item 148268076412.

rs1482680764 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13834268 (GRCh38)
19:13945082 (GRCh37)
Canonical SPDI:: NC_000019.10:13834267:C:T
Gene:: MIR23AHG (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.13834268C>T, NC_000019.9:g.13945082C>T, NW_021160022.1:g.46109C>T

Select item 148266721613.

rs1482667216 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13838063 (GRCh38)
19:13948877 (GRCh37)
Canonical SPDI:: NC_000019.10:13838062:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000054/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.13838063C>T, NC_000019.9:g.13948877C>T, NW_021160022.1:g.49904C>T, NR_036515.2:n.4856G>A

Select item 148238306114.

rs1482383061 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:13836819 (GRCh38)
19:13947633 (GRCh37)
Canonical SPDI:: NC_000019.10:13836818:A:G
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.13836819A>G, NC_000019.9:g.13947633A>G, NW_021160022.1:g.48660A>G, NR_036515.2:n.6100T>C

Select item 148235361015.

rs1482353610 [Homo sapiens]

Variant type:: DEL
Alleles:: GTAATCC>- [Show Flanks]
Chromosome:: 19:13837502 (GRCh38)
19:13948316 (GRCh37)
Canonical SPDI:: NC_000019.10:13837501:GTAATCC:
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000019.10:g.13837502_13837508del, NC_000019.9:g.13948316_13948322del, NW_021160022.1:g.49343_49349del, NR_036515.2:n.5411_5417del

Select item 148225699016.

rs1482256990 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:13834145 (GRCh38)
19:13944959 (GRCh37)
Canonical SPDI:: NC_000019.10:13834144:T:C
Gene:: MIR23AHG (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.13834145T>C, NC_000019.9:g.13944959T>C, NW_021160022.1:g.45986T>C

Select item 148200145317.

rs1482001453 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>- [Show Flanks]
Chromosome:: 19:13837935 (GRCh38)
19:13948749 (GRCh37)
Canonical SPDI:: NC_000019.10:13837933:CCC:C
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.13837935_13837936del, NC_000019.9:g.13948749_13948750del, NW_021160022.1:g.49776_49777del, NR_036515.2:n.4984_4985del

Select item 148136278618.

rs1481362786 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGAGGGGGGCACCGGG>- [Show Flanks]
Chromosome:: 19:13836671 (GRCh38)
19:13947485 (GRCh37)
Canonical SPDI:: NC_000019.10:13836667:GGGGTGAGGGGGGCACCGGG:GGG
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: -=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.13836671_13836687del, NC_000019.9:g.13947485_13947501del, NW_021160022.1:g.48512_48528del, NR_036515.2:n.6235_6251del

Select item 148054056819.

rs1480540568 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:13838282 (GRCh38)
19:13949096 (GRCh37)
Canonical SPDI:: NC_000019.10:13838281:C:T
Gene:: MIR23AHG (Varview), MIR23A (Varview), MIR24-2 (Varview), MIR27A (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.13838282C>T, NC_000019.9:g.13949096C>T, NW_021160022.1:g.50123C>T, NR_036515.2:n.4637G>A

Select item 148047314520.

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

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