SNP Links for Gene (Select 105378397) - SNP

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Select item 14914786691.

rs1491478669 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->GTTTTTTTTT
Chromosome:: no mapping
Canonical SPDI:

Select item 14914431532.

rs1491443153 has merged into rs200359835 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:83674573 (GRCh38)
10:85434329 (GRCh37)
Canonical SPDI:: NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:83674561:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTT=0./0 (GENOME_DK)
HGVS:: NC_000010.11:g.83674573_83674593del, NC_000010.11:g.83674575_83674593del, NC_000010.11:g.83674576_83674593del, NC_000010.11:g.83674577_83674593del, NC_000010.11:g.83674578_83674593del, NC_000010.11:g.83674579_83674593del, NC_000010.11:g.83674580_83674593del, NC_000010.11:g.83674581_83674593del, NC_000010.11:g.83674582_83674593del, NC_000010.11:g.83674583_83674593del, NC_000010.11:g.83674584_83674593del, NC_000010.11:g.83674585_83674593del, NC_000010.11:g.83674586_83674593del, NC_000010.11:g.83674587_83674593del, NC_000010.11:g.83674589_83674593del, NC_000010.11:g.83674590_83674593del, NC_000010.11:g.83674591_83674593del, NC_000010.11:g.83674592_83674593del, NC_000010.11:g.83674593del, NC_000010.11:g.83674593dup, NC_000010.11:g.83674592_83674593dup, NC_000010.11:g.83674591_83674593dup, NC_000010.11:g.83674590_83674593dup, NC_000010.11:g.83674589_83674593dup, NC_000010.11:g.83674588_83674593dup, NC_000010.11:g.83674587_83674593dup, NC_000010.11:g.83674586_83674593dup, NC_000010.11:g.83674585_83674593dup, NC_000010.11:g.83674584_83674593dup, NC_000010.11:g.83674583_83674593dup, NC_000010.11:g.83674582_83674593dup, NC_000010.11:g.83674581_83674593dup, NC_000010.11:g.83674580_83674593dup, NC_000010.11:g.83674579_83674593dup, NC_000010.11:g.83674578_83674593dup, NC_000010.11:g.83674576_83674593dup, NC_000010.11:g.83674575_83674593dup, NC_000010.11:g.83674574_83674593dup, NC_000010.11:g.83674573_83674593dup, NC_000010.11:g.83674572_83674593dup, NC_000010.11:g.83674570_83674593dup, NC_000010.11:g.83674569_83674593dup, NC_000010.11:g.83674568_83674593dup, NC_000010.11:g.83674567_83674593dup, NC_000010.10:g.85434329_85434349del, NC_000010.10:g.85434331_85434349del, NC_000010.10:g.85434332_85434349del, NC_000010.10:g.85434333_85434349del, NC_000010.10:g.85434334_85434349del, NC_000010.10:g.85434335_85434349del, NC_000010.10:g.85434336_85434349del, NC_000010.10:g.85434337_85434349del, NC_000010.10:g.85434338_85434349del, NC_000010.10:g.85434339_85434349del, NC_000010.10:g.85434340_85434349del, NC_000010.10:g.85434341_85434349del, NC_000010.10:g.85434342_85434349del, NC_000010.10:g.85434343_85434349del, NC_000010.10:g.85434345_85434349del, NC_000010.10:g.85434346_85434349del, NC_000010.10:g.85434347_85434349del, NC_000010.10:g.85434348_85434349del, NC_000010.10:g.85434349del, NC_000010.10:g.85434349dup, NC_000010.10:g.85434348_85434349dup, NC_000010.10:g.85434347_85434349dup, NC_000010.10:g.85434346_85434349dup, NC_000010.10:g.85434345_85434349dup, NC_000010.10:g.85434344_85434349dup, NC_000010.10:g.85434343_85434349dup, NC_000010.10:g.85434342_85434349dup, NC_000010.10:g.85434341_85434349dup, NC_000010.10:g.85434340_85434349dup, NC_000010.10:g.85434339_85434349dup, NC_000010.10:g.85434338_85434349dup, NC_000010.10:g.85434337_85434349dup, NC_000010.10:g.85434336_85434349dup, NC_000010.10:g.85434335_85434349dup, NC_000010.10:g.85434334_85434349dup, NC_000010.10:g.85434332_85434349dup, NC_000010.10:g.85434331_85434349dup, NC_000010.10:g.85434330_85434349dup, NC_000010.10:g.85434329_85434349dup, NC_000010.10:g.85434328_85434349dup, NC_000010.10:g.85434326_85434349dup, NC_000010.10:g.85434325_85434349dup, NC_000010.10:g.85434324_85434349dup, NC_000010.10:g.85434323_85434349dup

Select item 14908345803.

rs1490834580 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 10:83671979 (GRCh38)
10:85431735 (GRCh37)
Canonical SPDI:: NC_000010.11:83671978:TTTTT:TTTT
Gene:: LINC02650 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.83671983del, NC_000010.10:g.85431739del

Select item 14905836554.

rs1490583655 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:83676514 (GRCh38)
10:85436270 (GRCh37)
Canonical SPDI:: NC_000010.11:83676513:C:T
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.83676514C>T, NC_000010.10:g.85436270C>T

Select item 14892855925.

rs1489285592 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:83678403 (GRCh38)
10:85438159 (GRCh37)
Canonical SPDI:: NC_000010.11:83678402:C:T
Gene:: LINC02650 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.83678403C>T, NC_000010.10:g.85438159C>T

Select item 14885741166.

rs1488574116 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>C
Chromosome:: no mapping
Canonical SPDI:

Select item 14876963637.

rs1487696363 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTGTTTTTTTTTTTTTTTTT>- [Show Flanks]
Chromosome:: 10:83674559 (GRCh38)
10:85434315 (GRCh37)
Canonical SPDI:: NC_000010.11:83674555:TTTCTGTTTTTTTTTTTTTTTTT:TTT
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.83674559_83674578del, NC_000010.10:g.85434315_85434334del

Select item 14875220738.

rs1487522073 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:83672003 (GRCh38)
10:85431759 (GRCh37)
Canonical SPDI:: NC_000010.11:83672002:T:A
Gene:: LINC02650 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.83672003T>A, NC_000010.10:g.85431759T>A

Select item 14869928199.

rs1486992819 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:83677878 (GRCh38)
10:85437634 (GRCh37)
Canonical SPDI:: NC_000010.11:83677877:G:A
Gene:: LINC02650 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
HGVS:: NC_000010.11:g.83677878G>A, NC_000010.10:g.85437634G>A

Select item 148697287510.

rs1486972875 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:83677430 (GRCh38)
10:85437186 (GRCh37)
Canonical SPDI:: NC_000010.11:83677429:C:G,NC_000010.11:83677429:C:T
Gene:: LINC02650 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.83677430C>G, NC_000010.11:g.83677430C>T, NC_000010.10:g.85437186C>G, NC_000010.10:g.85437186C>T

Select item 148652365811.

rs1486523658 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:83672376 (GRCh38)
10:85432132 (GRCh37)
Canonical SPDI:: NC_000010.11:83672375:T:C
Gene:: LINC02650 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.83672376T>C, NC_000010.10:g.85432132T>C

Select item 148642606112.

rs1486426061 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:83676919 (GRCh38)
10:85436675 (GRCh37)
Canonical SPDI:: NC_000010.11:83676918:A:G
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.83676919A>G, NC_000010.10:g.85436675A>G

Select item 148628720313.

rs1486287203 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:83673472 (GRCh38)
10:85433228 (GRCh37)
Canonical SPDI:: NC_000010.11:83673471:G:A
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000010.11:g.83673472G>A, NC_000010.10:g.85433228G>A

Select item 148624093914.

rs1486240939 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:83673836 (GRCh38)
10:85433592 (GRCh37)
Canonical SPDI:: NC_000010.11:83673835:T:C
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_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_000010.11:g.83673836T>C, NC_000010.10:g.85433592T>C

Select item 148622412115.

rs1486224121 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:83674500 (GRCh38)
10:85434256 (GRCh37)
Canonical SPDI:: NC_000010.11:83674499:G:A,NC_000010.11:83674499:G:C
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.83674500G>A, NC_000010.11:g.83674500G>C, NC_000010.10:g.85434256G>A, NC_000010.10:g.85434256G>C

Select item 148599754416.

rs1485997544 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:83674548 (GRCh38)
10:85434304 (GRCh37)
Canonical SPDI:: NC_000010.11:83674547:C:A,NC_000010.11:83674547:C:T
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00084/9 (ALFA)
T=0.01164/34 (KOREAN)
HGVS:: NC_000010.11:g.83674548C>A, NC_000010.11:g.83674548C>T, NC_000010.10:g.85434304C>A, NC_000010.10:g.85434304C>T

Select item 148584077817.

rs1485840778 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:83675073 (GRCh38)
10:85434829 (GRCh37)
Canonical SPDI:: NC_000010.11:83675072:C:A
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.00005/7 (GnomAD)
HGVS:: NC_000010.11:g.83675073C>A, NC_000010.10:g.85434829C>A

Select item 148577045518.

rs1485770455 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 10:83676056 (GRCh38)
10:85435812 (GRCh37)
Canonical SPDI:: NC_000010.11:83676055:C:A,NC_000010.11:83676055:C:G
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.83676056C>A, NC_000010.11:g.83676056C>G, NC_000010.10:g.85435812C>A, NC_000010.10:g.85435812C>G

Select item 148555329219.

rs1485553292 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:83673031 (GRCh38)
10:85432787 (GRCh37)
Canonical SPDI:: NC_000010.11:83673030:A:G
Gene:: LINC02650 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.83673031A>G, NC_000010.10:g.85432787A>G

Select item 148518553420.

rs1485185534 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:83675412 (GRCh38)
10:85435168 (GRCh37)
Canonical SPDI:: NC_000010.11:83675411:A:C
Gene:: LINC02650 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000026/7 (TOPMED)
C=0.000043/6 (GnomAD)
HGVS:: NC_000010.11:g.83675412A>C, NC_000010.10:g.85435168A>C, NR_134317.1:n.187T>G

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