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rs1060501862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501862(A;A)
Make rs1060501862(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position35076970
GeneFANCG
is asnp
is mentioned by
dbSNPrs1060501862
dbSNP (old)rs1060501862
ClinGenrs1060501862
ebirs1060501862
HLIrs1060501862
Exacrs1060501862
Gnomadrs1060501862
Varsomers1060501862
Maprs1060501862
PheGenIrs1060501862
Biobankrs1060501862
1000 genomesrs1060501862
hgdprs1060501862
ensemblrs1060501862
gopubmedrs1060501862
geneviewrs1060501862
scholarrs1060501862
googlers1060501862
pharmgkbrs1060501862
gwascentralrs1060501862
openSNPrs1060501862
23andMers1060501862
23andMe allrs1060501862
SNPshotrs1060501862
SNPdbers1060501862
MSV3drs1060501862
GWAS Ctlgrs1060501862
Max Magnitude0
ClinVar
Risk rs1060501862(A;A)
Alt rs1060501862(A;A)
Reference Rs1060501862(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000009.11:g.35076967C>T
CLNSRC
CLNACC RCV000461878.1,