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rs786205573

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205573(A;A)
Make rs786205573(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position60890914
GeneERCC8
is asnp
is mentioned by
dbSNPrs786205573
ebirs786205573
HLIrs786205573
Exacrs786205573
Varsomers786205573
Maprs786205573
PheGenIrs786205573
hapmaprs786205573
1000 genomesrs786205573
hgdprs786205573
ensemblrs786205573
gopubmedrs786205573
geneviewrs786205573
scholarrs786205573
googlers786205573
pharmgkbrs786205573
gwascentralrs786205573
openSNPrs786205573
23andMers786205573
23andMe allrs786205573
SNP Nexus

SNPshotrs786205573
SNPdbers786205573
MSV3drs786205573
GWAS Ctlgrs786205573
Max Magnitude0
ClinVar
Risk rs786205573(A;A)
Alt rs786205573(A;A)
Reference rs786205573(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ERCC8
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.60186741C>T
CLNSRC
CLNACC RCV000171383.1,