SNP Links for Gene (Select 283682) - SNP

Links from Gene

Items: 1 to 20 of 10971

<< First< Prev

Page of 549

Next >Last >>

Select item 14915569801.

rs1491556980 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 15:93863245 (GRCh38)
15:94406474 (GRCh37)
Canonical SPDI:: NC_000015.10:93863244:AG:
Gene:: LINC02207 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000084/1 (ALFA)
-=0.000036/5 (GnomAD)
-=0.000045/12 (TOPMED)
HGVS:: NC_000015.10:g.93863245_93863246del, NC_000015.9:g.94406474_94406475del

Select item 14914255682.

rs1491425568 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 15:93890807 (GRCh38)
15:94434036 (GRCh37)
Canonical SPDI:: NC_000015.10:93890805:ACA:A
Validated:: by frequency,by alfa
MAF:: A=0.000054/1 (ALFA)
-=0.00005/7 (GnomAD)
HGVS:: NC_000015.10:g.93890807_93890808del, NC_000015.9:g.94434036_94434037del

Select item 14912610143.

rs1491261014 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 15:93855139 (GRCh38)
15:94398369 (GRCh37)
Canonical SPDI:: NC_000015.10:93855139:A:AA
Gene:: LINC02207 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
A=0.000015/2 (GnomAD)
HGVS:: NC_000015.10:g.93855140dup, NC_000015.9:g.94398369dup

Select item 14911033244.

rs1491103324 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 15:93855140 (GRCh38)
15:94398369 (GRCh37)
Canonical SPDI:: NC_000015.10:93855138:TAT:T
Gene:: LINC02207 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000023/3 (GnomAD)
HGVS:: NC_000015.10:g.93855140_93855141del, NC_000015.9:g.94398369_94398370del

Select item 14910428925.

rs1491042892 has merged into rs55651047 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA [Show Flanks]
Chromosome:: 15:93890804 (GRCh38)
15:94434033 (GRCh37)
Canonical SPDI:: NC_000015.10:93890794:AAAAAAAAAAAA:AAAAAAAAA,NC_000015.10:93890794:AAAAAAAAAAAA:AAAAAAAAAA,NC_000015.10:93890794:AAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:93890794:AAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:93890794:AAAAAAAAAAAA:AAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.16721/620 (TWINSUK)
-=0.18293/705 (ALSPAC)
-=0.1935/804 (1000Genomes)
HGVS:: NC_000015.10:g.93890804_93890806del, NC_000015.10:g.93890805_93890806del, NC_000015.10:g.93890806del, NC_000015.10:g.93890806dup, NC_000015.10:g.93890805_93890806dup, NC_000015.9:g.94434033_94434035del, NC_000015.9:g.94434034_94434035del, NC_000015.9:g.94434035del, NC_000015.9:g.94434035dup, NC_000015.9:g.94434034_94434035dup

Select item 14910207286.

rs1491020728 [Homo sapiens]

Variant type:: DEL
Alleles:: GC>- [Show Flanks]
Chromosome:: 15:93882446 (GRCh38)
15:94425675 (GRCh37)
Canonical SPDI:: NC_000015.10:93882445:GC:
Validated:: by frequency
MAF:: -=0.0003/30 (GnomAD)
HGVS:: NC_000015.10:g.93882446_93882447del, NC_000015.9:g.94425675_94425676del

Select item 14910061987.

rs1491006198 has merged into rs72123421 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 15:93882458 (GRCh38)
15:94425687 (GRCh37)
Canonical SPDI:: NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:93882447:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000015.10:g.93882458_93882463del, NC_000015.10:g.93882460_93882463del, NC_000015.10:g.93882461_93882463del, NC_000015.10:g.93882462_93882463del, NC_000015.10:g.93882463del, NC_000015.10:g.93882463dup, NC_000015.10:g.93882462_93882463dup, NC_000015.10:g.93882461_93882463dup, NC_000015.10:g.93882454_93882463dup, NC_000015.10:g.93882463_93882464insAAAAAAAAAAAAAAAAA, NC_000015.9:g.94425687_94425692del, NC_000015.9:g.94425689_94425692del, NC_000015.9:g.94425690_94425692del, NC_000015.9:g.94425691_94425692del, NC_000015.9:g.94425692del, NC_000015.9:g.94425692dup, NC_000015.9:g.94425691_94425692dup, NC_000015.9:g.94425690_94425692dup, NC_000015.9:g.94425683_94425692dup, NC_000015.9:g.94425692_94425693insAAAAAAAAAAAAAAAAA

Select item 14908922888.

rs1490892288 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:93884447 (GRCh38)
15:94427676 (GRCh37)
Canonical SPDI:: NC_000015.10:93884446:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.93884447G>A, NC_000015.9:g.94427676G>A

Select item 14908277709.

rs1490827770 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:93876355 (GRCh38)
15:94419584 (GRCh37)
Canonical SPDI:: NC_000015.10:93876354:T:A
Gene:: LINC02207 (Varview)
Functional Consequence:: intron_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_000015.10:g.93876355T>A, NC_000015.9:g.94419584T>A

Select item 149082652010.

rs1490826520 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:93898024 (GRCh38)
15:94441253 (GRCh37)
Canonical SPDI:: NC_000015.10:93898023:C:T
Gene:: LINC01579 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.93898024C>T, NC_000015.9:g.94441253C>T

Select item 149081094811.

rs1490810948 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:93900149 (GRCh38)
15:94443378 (GRCh37)
Canonical SPDI:: NC_000015.10:93900148:G:A
Gene:: LINC01579 (Varview), LINC01580 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.93900149G>A, NC_000015.9:g.94443378G>A

Select item 149080120512.

rs1490801205 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:93877477 (GRCh38)
15:94420706 (GRCh37)
Canonical SPDI:: NC_000015.10:93877476:T:A
Gene:: LINC02207 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.93877477T>A, NC_000015.9:g.94420706T>A

Select item 149076377213.

rs1490763772 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAT [Show Flanks]
Chromosome:: 15:93892494 (GRCh38)
15:94435724 (GRCh37)
Canonical SPDI:: NC_000015.10:93892494:TTAT:TTATTAT
Validated:: by frequency,by alfa
MAF:: TTATTAT=0./0 (ALFA)
TTA=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.93892496_93892498dup, NC_000015.9:g.94435725_94435727dup

Select item 149074836214.

rs1490748362 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:93893675 (GRCh38)
15:94436904 (GRCh37)
Canonical SPDI:: NC_000015.10:93893674:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.93893675C>T, NC_000015.9:g.94436904C>T

Select item 149069824915.

rs1490698249 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:93851866 (GRCh38)
15:94395095 (GRCh37)
Canonical SPDI:: NC_000015.10:93851865:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.93851866C>T, NC_000015.9:g.94395095C>T

Select item 149062334216.

rs1490623342 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 15:93882590 (GRCh38)
15:94425820 (GRCh37)
Canonical SPDI:: NC_000015.10:93882590:T:TT
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.93882591dup, NC_000015.9:g.94425820dup

Select item 149043153517.

rs1490431535 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:93868910 (GRCh38)
15:94412139 (GRCh37)
Canonical SPDI:: NC_000015.10:93868909:G:A
Gene:: LINC02207 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000015.10:g.93868910G>A, NC_000015.9:g.94412139G>A

Select item 149033807118.

rs1490338071 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 15:93875980 (GRCh38)
15:94419209 (GRCh37)
Canonical SPDI:: NC_000015.10:93875979:T:C,NC_000015.10:93875979:T:G
Gene:: LINC02207 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.93875980T>C, NC_000015.10:g.93875980T>G, NC_000015.9:g.94419209T>C, NC_000015.9:g.94419209T>G

Select item 149033395919.

rs1490333959 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:93899154 (GRCh38)
15:94442383 (GRCh37)
Canonical SPDI:: NC_000015.10:93899153:C:G
Gene:: LINC01579 (Varview), LINC01580 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000015.10:g.93899154C>G, NC_000015.9:g.94442383C>G

Select item 149031967420.

rs1490319674 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:93866613 (GRCh38)
15:94409842 (GRCh37)
Canonical SPDI:: NC_000015.10:93866612:T:C
Gene:: LINC02207 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.93866613T>C, NC_000015.9:g.94409842T>C

<< First< Prev

Page of 549

Next >Last >>

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 10971

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity