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rs61760163

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61760163(A;A)
Make rs61760163(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position49482860
GeneERCC6
is asnp
is mentioned by
dbSNPrs61760163
ebirs61760163
HLIrs61760163
Exacrs61760163
Varsomers61760163
Maprs61760163
PheGenIrs61760163
hapmaprs61760163
1000 genomesrs61760163
hgdprs61760163
ensemblrs61760163
gopubmedrs61760163
geneviewrs61760163
scholarrs61760163
googlers61760163
pharmgkbrs61760163
gwascentralrs61760163
openSNPrs61760163
23andMers61760163
23andMe allrs61760163
SNP Nexus

SNPshotrs61760163
SNPdbers61760163
MSV3drs61760163
GWAS Ctlgrs61760163
Max Magnitude0
ClinVar
Risk rs61760163(A;A)
Alt rs61760163(A;A)
Reference rs61760163(G;G)
Significance Pathogenic
Disease not specified not provided Cockayne syndrome B
Variation info
Gene ERCC6
CLNDBN not specified not provided Cockayne syndrome B
Reversed 0
HGVS NC_000010.10:g.50690906G>A
CLNSRC
CLNACC RCV000170374.2, RCV000173644.1, RCV000234812.1,