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rs774209201

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774209201(C;G)
Make rs774209201(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95126582
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs774209201
ebirs774209201
HLIrs774209201
Exacrs774209201
Varsomers774209201
Maprs774209201
PheGenIrs774209201
hapmaprs774209201
1000 genomesrs774209201
hgdprs774209201
ensemblrs774209201
gopubmedrs774209201
geneviewrs774209201
scholarrs774209201
googlers774209201
pharmgkbrs774209201
gwascentralrs774209201
openSNPrs774209201
23andMers774209201
23andMe allrs774209201
SNP Nexus

SNPshotrs774209201
SNPdbers774209201
MSV3drs774209201
GWAS Ctlgrs774209201
Max Magnitude0
ClinVar
Risk rs774209201(G;G)
Alt rs774209201(G;G)
Reference rs774209201(C;C)
Significance Pathogenic
Disease Fanconi anemia not provided
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C not provided
Reversed 0
HGVS NC_000009.11:g.97888864C>G
CLNSRC
CLNACC RCV000169449.1, RCV000224795.1,