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rs254942

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs254942(C;T)
Make rs254942(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position13932150
GeneERCC4
is asnp
is mentioned by
dbSNPrs254942
dbSNP (old)rs254942
ClinGenrs254942
ebirs254942
HLIrs254942
Exacrs254942
Gnomadrs254942
Varsomers254942
Maprs254942
PheGenIrs254942
Biobankrs254942
1000 genomesrs254942
hgdprs254942
ensemblrs254942
gopubmedrs254942
geneviewrs254942
scholarrs254942
googlers254942
pharmgkbrs254942
gwascentralrs254942
openSNPrs254942
23andMers254942
23andMe allrs254942
SNP Nexus

SNPshotrs254942
SNPdbers254942
MSV3drs254942
GWAS Ctlgrs254942
GMAF0.06933
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 23415627] Association of two ERCC4 tagSNPs with susceptibility to atrophic gastritis and gastric cancer in Chinese


ClinVar
Risk rs254942(A;A) rs254942(T;T)
Alt rs254942(A;A) rs254942(T;T)
Reference Rs254942(C;C)
Significance Non-pathogenic
Disease not specified Xeroderma pigmentosum
Variation info
Gene ERCC4
CLNDBN not specified Xeroderma pigmentosum
Reversed 1
HGVS NC_000016.9:g.14026007G>A
CLNSRC
CLNACC RCV000246561.1, RCV000318579.1,