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rs370510954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370510954(A;A)
Make rs370510954(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position95125085
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs370510954
dbSNP (classic)rs370510954
ClinGenrs370510954
ebirs370510954
HLIrs370510954
Exacrs370510954
Gnomadrs370510954
Varsomers370510954
LitVarrs370510954
Maprs370510954
PheGenIrs370510954
Biobankrs370510954
1000 genomesrs370510954
hgdprs370510954
ensemblrs370510954
geneviewrs370510954
scholarrs370510954
googlers370510954
pharmgkbrs370510954
gwascentralrs370510954
openSNPrs370510954
23andMers370510954
23andMe allrs370510954
SNPshotrs370510954
SNPdbers370510954
MSV3drs370510954
GWAS Ctlgrs370510954
Max Magnitude0
ClinVar
Risk rs370510954(A;A)
Alt rs370510954(A;A)
Reference Rs370510954(C;C)
Significance Probable-Pathogenic
Disease not provided Fanconi anemia Fanconi anemia
Variation info
Gene FANCC
CLNDBN not provided Fanconi anemia, complementation group C Fanconi anemia
Reversed 0
HGVS NC_000009.11:g.97887367C>A
CLNSRC
CLNACC RCV000254963.2, RCV000412116.1, RCV000458747.1,