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rs371897078

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371897078(C;T)
Make rs371897078(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95111630
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs371897078
ebirs371897078
HLIrs371897078
Exacrs371897078
Varsomers371897078
Maprs371897078
PheGenIrs371897078
hapmaprs371897078
1000 genomesrs371897078
hgdprs371897078
ensemblrs371897078
gopubmedrs371897078
geneviewrs371897078
scholarrs371897078
googlers371897078
pharmgkbrs371897078
gwascentralrs371897078
openSNPrs371897078
23andMers371897078
23andMe allrs371897078
SNP Nexus

SNPshotrs371897078
SNPdbers371897078
MSV3drs371897078
GWAS Ctlgrs371897078
Max Magnitude0
ClinVar
Risk rs371897078(T;T)
Alt rs371897078(T;T)
Reference rs371897078(C;C)
Significance Pathogenic
Disease not provided Fanconi anemia
Variation info
Gene FANCC
CLNDBN not provided Fanconi anemia
Reversed 0
HGVS NC_000009.11:g.97873912C>A; NC_000009.11:g.97873912C>T
CLNSRC
CLNACC RCV000202668.1, RCV000205129.1,