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rs876661231

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661231(G;T)
Make rs876661231(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position95172105
GeneFANCC
is asnp
is mentioned by
dbSNPrs876661231
ebirs876661231
HLIrs876661231
Exacrs876661231
Varsomers876661231
Maprs876661231
PheGenIrs876661231
hapmaprs876661231
1000 genomesrs876661231
hgdprs876661231
ensemblrs876661231
gopubmedrs876661231
geneviewrs876661231
scholarrs876661231
googlers876661231
pharmgkbrs876661231
gwascentralrs876661231
openSNPrs876661231
23andMers876661231
23andMe allrs876661231
SNP Nexus

SNPshotrs876661231
SNPdbers876661231
MSV3drs876661231
GWAS Ctlgrs876661231
Max Magnitude0
ClinVar
Risk rs876661231(T;T)
Alt rs876661231(T;T)
Reference rs876661231(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.97934387C>A
CLNSRC
CLNACC RCV000219758.1,