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rs149616199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149616199(C;G)
Make rs149616199(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35075278
GeneFANCG
is asnp
is mentioned by
dbSNPrs149616199
ebirs149616199
HLIrs149616199
Exacrs149616199
Varsomers149616199
Maprs149616199
PheGenIrs149616199
hapmaprs149616199
1000 genomesrs149616199
hgdprs149616199
ensemblrs149616199
gopubmedrs149616199
geneviewrs149616199
scholarrs149616199
googlers149616199
pharmgkbrs149616199
gwascentralrs149616199
openSNPrs149616199
23andMers149616199
23andMe allrs149616199
SNP Nexus

SNPshotrs149616199
SNPdbers149616199
MSV3drs149616199
GWAS Ctlgrs149616199
Max Magnitude0
ClinVar
Risk rs149616199(G;G)
Alt rs149616199(G;G)
Reference rs149616199(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 0
HGVS NC_000009.11:g.35075275C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007109.3,