SNP Links for Gene (Select 406981) - SNP

Links from Gene

Items: 1 to 20 of 464

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Select item 14905161251.

rs1490516125 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:134170283 (GRCh38)
X:133304313 (GRCh37)
Canonical SPDI:: NC_000023.11:134170282:T:C
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.134170283T>C, NC_000023.10:g.133304313T>C, XR_007068340.1:n.2490A>G

Select item 14898230842.

rs1489823084 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:134171426 (GRCh38)
X:133305456 (GRCh37)
Canonical SPDI:: NC_000023.11:134171425:T:A
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.134171426T>A, NC_000023.10:g.133305456T>A

Select item 14891889163.

rs1489188916 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:134169223 (GRCh38)
X:133303253 (GRCh37)
Canonical SPDI:: NC_000023.11:134169222:G:A,NC_000023.11:134169222:G:C
Gene:: MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.134169223G>A, NC_000023.11:g.134169223G>C, NC_000023.10:g.133303253G>A, NC_000023.10:g.133303253G>C, XR_007068340.1:n.3550C>T, XR_007068340.1:n.3550C>G

Select item 14878941544.

rs1487894154 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:134169800 (GRCh38)
X:133303830 (GRCh37)
Canonical SPDI:: NC_000023.11:134169799:T:C
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000006/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.134169800T>C, NC_000023.10:g.133303830T>C, XR_007068340.1:n.2973A>G

Select item 14789332145.

rs1478933214 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:134170645 (GRCh38)
X:133304675 (GRCh37)
Canonical SPDI:: NC_000023.11:134170644:T:C
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.134170645T>C, NC_000023.10:g.133304675T>C

Select item 14778441746.

rs1477844174 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:134170218 (GRCh38)
X:133304248 (GRCh37)
Canonical SPDI:: NC_000023.11:134170217:C:T
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.134170218C>T, NC_000023.10:g.133304248C>T, XR_007068340.1:n.2555G>A, NR_029523.1:n.61G>A

Select item 14726713117.

rs1472671311 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:134169587 (GRCh38)
X:133303617 (GRCh37)
Canonical SPDI:: NC_000023.11:134169586:T:C
Gene:: MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.134169587T>C, NC_000023.10:g.133303617T>C, XR_007068340.1:n.3186A>G, NR_029509.1:n.26A>G

Select item 14725650928.

rs1472565092 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:134170140 (GRCh38)
X:133304170 (GRCh37)
Canonical SPDI:: NC_000023.11:134170139:A:G
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000006/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.134170140A>G, NC_000023.10:g.133304170A>G, XR_007068340.1:n.2633T>C

Select item 14716880799.

rs1471688079 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:134170180 (GRCh38)
X:133304210 (GRCh37)
Canonical SPDI:: NC_000023.11:134170179:T:C
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.134170180T>C, NC_000023.10:g.133304210T>C, XR_007068340.1:n.2593A>G

Select item 146815221110.

rs1468152211 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:134171247 (GRCh38)
X:133305277 (GRCh37)
Canonical SPDI:: NC_000023.11:134171246:A:G
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
G=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.134171247A>G, NC_000023.10:g.133305277A>G

Select item 146621083311.

rs1466210833 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:134170130 (GRCh38)
X:133304160 (GRCh37)
Canonical SPDI:: NC_000023.11:134170129:G:A
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000006/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.134170130G>A, NC_000023.10:g.133304160G>A, XR_007068340.1:n.2643C>T

Select item 146549115412.

rs1465491154 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:134169613 (GRCh38)
X:133303643 (GRCh37)
Canonical SPDI:: NC_000023.11:134169612:A:T
Gene:: MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.134169613A>T, NC_000023.10:g.133303643A>T, XR_007068340.1:n.3160T>A

Select item 146419522213.

rs1464195222 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:134170698 (GRCh38)
X:133304728 (GRCh37)
Canonical SPDI:: NC_000023.11:134170697:G:C
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.134170698G>C, NC_000023.10:g.133304728G>C

Select item 146375162914.

rs1463751629 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:134169769 (GRCh38)
X:133303799 (GRCh37)
Canonical SPDI:: NC_000023.11:134169768:T:C
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.134169769T>C, NC_000023.10:g.133303799T>C, XR_007068340.1:n.3004A>G

Select item 146345607515.

rs1463456075 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:134170011 (GRCh38)
X:133304041 (GRCh37)
Canonical SPDI:: NC_000023.11:134170010:C:T
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.134170011C>T, NC_000023.10:g.133304041C>T, XR_007068340.1:n.2762G>A

Select item 146287270116.

rs1462872701 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: X:134171314 (GRCh38)
X:133305344 (GRCh37)
Canonical SPDI:: NC_000023.11:134171313:A:C,NC_000023.11:134171313:A:G
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000029/3 (GnomAD)
G=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.134171314A>C, NC_000023.11:g.134171314A>G, NC_000023.10:g.133305344A>C, NC_000023.10:g.133305344A>G

Select item 146027716317.

rs1460277163 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:134170684 (GRCh38)
X:133304714 (GRCh37)
Canonical SPDI:: NC_000023.11:134170683:G:A
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.134170684G>A, NC_000023.10:g.133304714G>A

Select item 145785797718.

rs1457857977 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:134170560 (GRCh38)
X:133304590 (GRCh37)
Canonical SPDI:: NC_000023.11:134170559:C:T
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0.000224/1 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.134170560C>T, NC_000023.10:g.133304590C>T

Select item 145768615019.

rs1457686150 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:134169447 (GRCh38)
X:133303477 (GRCh37)
Canonical SPDI:: NC_000023.11:134169446:A:C
Gene:: MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), LOC124905221 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
HGVS:: NC_000023.11:g.134169447A>C, NC_000023.10:g.133303477A>C, XR_007068340.1:n.3326T>G, NR_029852.1:n.6T>G

Select item 145542495320.

rs1455424953 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: X:134170746 (GRCh38)
X:133304776 (GRCh37)
Canonical SPDI:: NC_000023.11:134170745:C:A,NC_000023.11:134170745:C:G,NC_000023.11:134170745:C:T
Gene:: MIR106A (Varview), MIR19B2 (Varview), MIR92A2 (Varview), MIR363 (Varview), MIR20B (Varview), MIR18B (Varview), LOC124905221 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.134170746C>A, NC_000023.11:g.134170746C>G, NC_000023.11:g.134170746C>T, NC_000023.10:g.133304776C>A, NC_000023.10:g.133304776C>G, NC_000023.10:g.133304776C>T

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