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rs370974124

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370974124(A;A)
Make rs370974124(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position95101721
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs370974124
ebirs370974124
HLIrs370974124
Exacrs370974124
Varsomers370974124
Maprs370974124
PheGenIrs370974124
hapmaprs370974124
1000 genomesrs370974124
hgdprs370974124
ensemblrs370974124
gopubmedrs370974124
geneviewrs370974124
scholarrs370974124
googlers370974124
pharmgkbrs370974124
gwascentralrs370974124
openSNPrs370974124
23andMers370974124
23andMe allrs370974124
SNP Nexus

SNPshotrs370974124
SNPdbers370974124
MSV3drs370974124
GWAS Ctlgrs370974124
Max Magnitude0
ClinVar
Risk rs370974124(A,T;A,T)
Alt rs370974124(A,T;A,T)
Reference rs370974124(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.97864003G>A
CLNSRC
CLNACC RCV000218828.1,