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rs786205171

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205171(-;-)
Make rs786205171(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position49470424
GeneERCC6, LOC105378300
is asnp
is mentioned by
dbSNPrs786205171
ebirs786205171
HLIrs786205171
Exacrs786205171
Varsomers786205171
Maprs786205171
PheGenIrs786205171
hapmaprs786205171
1000 genomesrs786205171
hgdprs786205171
ensemblrs786205171
gopubmedrs786205171
geneviewrs786205171
scholarrs786205171
googlers786205171
pharmgkbrs786205171
gwascentralrs786205171
openSNPrs786205171
23andMers786205171
23andMe allrs786205171
SNP Nexus

SNPshotrs786205171
SNPdbers786205171
MSV3drs786205171
GWAS Ctlgrs786205171
Max Magnitude0
ClinVar
Risk rs786205171(;)
Alt rs786205171(;)
Reference rs786205171(A;A)
Significance Pathogenic
Disease Cockayne syndrome B not provided
Variation info
Gene ERCC6
CLNDBN Cockayne syndrome B not provided
Reversed 1
HGVS NC_000010.10:g.50678470delT
CLNSRC
CLNACC RCV000170386.1, RCV000224382.1,