Have questions? Visit https://www.reddit.com/r/SNPedia

rs145394391

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145394391(C;T)
Make rs145394391(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position95171078
GeneFANCC
is asnp
is mentioned by
dbSNPrs145394391
ebirs145394391
HLIrs145394391
Exacrs145394391
Varsomers145394391
Maprs145394391
PheGenIrs145394391
hapmaprs145394391
1000 genomesrs145394391
hgdprs145394391
ensemblrs145394391
gopubmedrs145394391
geneviewrs145394391
scholarrs145394391
googlers145394391
pharmgkbrs145394391
gwascentralrs145394391
openSNPrs145394391
23andMers145394391
23andMe allrs145394391
SNP Nexus

SNPshotrs145394391
SNPdbers145394391
MSV3drs145394391
GWAS Ctlgrs145394391
Max Magnitude0
ClinVar
Risk rs145394391(T;T)
Alt rs145394391(T;T)
Reference rs145394391(C;C)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000009.11:g.97933360C>T
CLNSRC
CLNACC RCV000230742.1,