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rs368728467

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs368728467(A;G)
Make rs368728467(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position49474074
GeneERCC6
is asnp
is mentioned by
dbSNPrs368728467
ebirs368728467
HLIrs368728467
Exacrs368728467
Varsomers368728467
Maprs368728467
PheGenIrs368728467
hapmaprs368728467
1000 genomesrs368728467
hgdprs368728467
ensemblrs368728467
gopubmedrs368728467
geneviewrs368728467
scholarrs368728467
googlers368728467
pharmgkbrs368728467
gwascentralrs368728467
openSNPrs368728467
23andMers368728467
23andMe allrs368728467
SNP Nexus

SNPshotrs368728467
SNPdbers368728467
MSV3drs368728467
GWAS Ctlgrs368728467
Max Magnitude0
ClinVar
Risk rs368728467(G;G)
Alt rs368728467(G;G)
Reference rs368728467(A;A)
Significance Pathogenic
Disease Cockayne syndrome B
Variation info
Gene ERCC6
CLNDBN Cockayne syndrome B
Reversed 0
HGVS NC_000010.10:g.50682120A>G
CLNSRC
CLNACC RCV000195010.1,