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rs786204205

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204205(G;T)
Make rs786204205(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position35074384
GeneFANCG, VCP
is asnp
is mentioned by
dbSNPrs786204205
ebirs786204205
HLIrs786204205
Exacrs786204205
Varsomers786204205
Maprs786204205
PheGenIrs786204205
hapmaprs786204205
1000 genomesrs786204205
hgdprs786204205
ensemblrs786204205
gopubmedrs786204205
geneviewrs786204205
scholarrs786204205
googlers786204205
pharmgkbrs786204205
gwascentralrs786204205
openSNPrs786204205
23andMers786204205
23andMe allrs786204205
SNP Nexus

SNPshotrs786204205
SNPdbers786204205
MSV3drs786204205
GWAS Ctlgrs786204205
Max Magnitude0
ClinVar
Risk rs786204205(T;T)
Alt rs786204205(T;T)
Reference rs786204205(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene VCP FANCG
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.35074381C>A
CLNSRC
CLNACC RCV000168294.2,