Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205168

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205168(-;-)
Make rs786205168(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position49505892
GeneERCC6
is asnp
is mentioned by
dbSNPrs786205168
ebirs786205168
HLIrs786205168
Exacrs786205168
Varsomers786205168
Maprs786205168
PheGenIrs786205168
hapmaprs786205168
1000 genomesrs786205168
hgdprs786205168
ensemblrs786205168
gopubmedrs786205168
geneviewrs786205168
scholarrs786205168
googlers786205168
pharmgkbrs786205168
gwascentralrs786205168
openSNPrs786205168
23andMers786205168
23andMe allrs786205168
SNP Nexus

SNPshotrs786205168
SNPdbers786205168
MSV3drs786205168
GWAS Ctlgrs786205168
Max Magnitude0
ClinVar
Risk rs786205168(;)
Alt rs786205168(;)
Reference rs786205168(G;G)
Significance Probable-Pathogenic
Disease Cockayne syndrome B
Variation info
Gene ERCC6
CLNDBN Cockayne syndrome B
Reversed 1
HGVS NC_000010.10:g.50713938delC
CLNSRC
CLNACC RCV000170368.1,