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

rs147105770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147105770(C;T)
Make rs147105770(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position13935697
GeneERCC4
is asnp
is mentioned by
dbSNPrs147105770
ebirs147105770
HLIrs147105770
Exacrs147105770
Varsomers147105770
Maprs147105770
PheGenIrs147105770
hapmaprs147105770
1000 genomesrs147105770
hgdprs147105770
ensemblrs147105770
gopubmedrs147105770
geneviewrs147105770
scholarrs147105770
googlers147105770
pharmgkbrs147105770
gwascentralrs147105770
openSNPrs147105770
23andMers147105770
23andMe allrs147105770
SNP Nexus

SNPshotrs147105770
SNPdbers147105770
MSV3drs147105770
GWAS Ctlgrs147105770
Max Magnitude0
ClinVar
Risk rs147105770(T;T)
Alt rs147105770(T;T)
Reference rs147105770(C;C)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene ERCC4
CLNDBN Xeroderma pigmentosum, type f/Cockayne syndrome
Reversed 0
HGVS NC_000016.9:g.14029554C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049250.27,