SNP Links for Gene (Select 7190) - SNP

Links from Gene

Items: 1 to 20 of 1251

<< First< Prev

Page of 63

Next >Last >>

Select item 14905643391.

rs1490564339 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:99257424 (GRCh38)
15:99797629 (GRCh37)
Canonical SPDI:: NC_000015.10:99257423:A:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
G=0.000057/8 (GnomAD)
HGVS:: NC_000015.10:g.99257424A>G, NC_000015.9:g.99797629A>G

Select item 14902352322.

rs1490235232 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:99259651 (GRCh38)
15:99799856 (GRCh37)
Canonical SPDI:: NC_000015.10:99259650:G:A
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000042/11 (TOPMED)
A=0.000043/6 (GnomAD)
HGVS:: NC_000015.10:g.99259651G>A, NC_000015.9:g.99799856G>A, NR_073383.1:n.2127G>A

Select item 14900767143.

rs1490076714 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:99257103 (GRCh38)
15:99797308 (GRCh37)
Canonical SPDI:: NC_000015.10:99257102:A:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000015.10:g.99257103A>G, NC_000015.9:g.99797308A>G

Select item 14894266124.

rs1489426612 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:99259679 (GRCh38)
15:99799884 (GRCh37)
Canonical SPDI:: NC_000015.10:99259678:C:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
HGVS:: NC_000015.10:g.99259679C>T, NC_000015.9:g.99799884C>T, NR_073383.1:n.2155C>T

Select item 14889614675.

rs1488961467 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:99259861 (GRCh38)
15:99800066 (GRCh37)
Canonical SPDI:: NC_000015.10:99259860:T:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.99259861T>G, NC_000015.9:g.99800066T>G, NR_073383.1:n.2337T>G

Select item 14887555536.

rs1488755553 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:99257510 (GRCh38)
15:99797715 (GRCh37)
Canonical SPDI:: NC_000015.10:99257509:A:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.99257510A>G, NC_000015.9:g.99797715A>G

Select item 14881899647.

rs1488189964 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 15:99259310 (GRCh38)
15:99799515 (GRCh37)
Canonical SPDI:: NC_000015.10:99259309:A:G,NC_000015.10:99259309:A:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.99259310A>G, NC_000015.10:g.99259310A>T, NC_000015.9:g.99799515A>G, NC_000015.9:g.99799515A>T, NR_073383.1:n.1786A>G, NR_073383.1:n.1786A>T

Select item 14872094808.

rs1487209480 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:99258792 (GRCh38)
15:99798997 (GRCh37)
Canonical SPDI:: NC_000015.10:99258791:T:C
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.99258792T>C, NC_000015.9:g.99798997T>C, NR_073383.1:n.1268T>C

Select item 14871227819.

rs1487122781 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:99257855 (GRCh38)
15:99798060 (GRCh37)
Canonical SPDI:: NC_000015.10:99257854:G:A
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.99257855G>A, NC_000015.9:g.99798060G>A, NR_073383.1:n.331G>A

Select item 148700618810.

rs1487006188 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:99257587 (GRCh38)
15:99797792 (GRCh37)
Canonical SPDI:: NC_000015.10:99257586:C:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_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=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.99257587C>T, NC_000015.9:g.99797792C>T, NR_073383.1:n.63C>T

Select item 148555420211.

rs1485554202 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:99257388 (GRCh38)
15:99797593 (GRCh37)
Canonical SPDI:: NC_000015.10:99257387:A:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000015.10:g.99257388A>G, NC_000015.9:g.99797593A>G

Select item 148417427012.

rs1484174270 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:99259352 (GRCh38)
15:99799557 (GRCh37)
Canonical SPDI:: NC_000015.10:99259351:C:G,NC_000015.10:99259351:C:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.99259352C>G, NC_000015.10:g.99259352C>T, NC_000015.9:g.99799557C>G, NC_000015.9:g.99799557C>T, NR_073383.1:n.1828C>G, NR_073383.1:n.1828C>T

Select item 148370367013.

rs1483703670 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:99258489 (GRCh38)
15:99798694 (GRCh37)
Canonical SPDI:: NC_000015.10:99258488:G:A
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.99258489G>A, NC_000015.9:g.99798694G>A, NR_073383.1:n.965G>A

Select item 148241660414.

rs1482416604 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:99259146 (GRCh38)
15:99799351 (GRCh37)
Canonical SPDI:: NC_000015.10:99259145:G:A
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000015.10:g.99259146G>A, NC_000015.9:g.99799351G>A, NR_073383.1:n.1622G>A

Select item 148218496215.

rs1482184962 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:99255593 (GRCh38)
15:99795798 (GRCh37)
Canonical SPDI:: NC_000015.10:99255592:G:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,genic_upstream_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)
HGVS:: NC_000015.10:g.99255593G>T, NC_000015.9:g.99795798G>T

Select item 148153016816.

rs1481530168 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:99256207 (GRCh38)
15:99796412 (GRCh37)
Canonical SPDI:: NC_000015.10:99256206:C:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.99256207C>T, NC_000015.9:g.99796412C>T

Select item 148145884917.

rs1481458849 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:99257294 (GRCh38)
15:99797499 (GRCh37)
Canonical SPDI:: NC_000015.10:99257293:T:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000015.10:g.99257294T>G, NC_000015.9:g.99797499T>G

Select item 148045038118.

rs1480450381 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:99256197 (GRCh38)
15:99796402 (GRCh37)
Canonical SPDI:: NC_000015.10:99256196:C:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_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_000015.10:g.99256197C>T, NC_000015.9:g.99796402C>T

Select item 148025899219.

rs1480258992 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:99259449 (GRCh38)
15:99799654 (GRCh37)
Canonical SPDI:: NC_000015.10:99259448:A:G
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_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_000015.10:g.99259449A>G, NC_000015.9:g.99799654A>G, NR_073383.1:n.1925A>G

Select item 147964947020.

rs1479649470 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:99259620 (GRCh38)
15:99799825 (GRCh37)
Canonical SPDI:: NC_000015.10:99259619:C:T
Gene:: HSP90B2P (Varview), LRRC28 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000042/11 (TOPMED)
T=0.000177/3 (TOMMO)
HGVS:: NC_000015.10:g.99259620C>T, NC_000015.9:g.99799825C>T, NR_073383.1:n.2096C>T

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1251

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity