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

rs766105286

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766105286(A;A)
Make rs766105286(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95111502
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs766105286
ebirs766105286
HLIrs766105286
Exacrs766105286
Varsomers766105286
Maprs766105286
PheGenIrs766105286
hapmaprs766105286
1000 genomesrs766105286
hgdprs766105286
ensemblrs766105286
gopubmedrs766105286
geneviewrs766105286
scholarrs766105286
googlers766105286
pharmgkbrs766105286
gwascentralrs766105286
openSNPrs766105286
23andMers766105286
23andMe allrs766105286
SNP Nexus

SNPshotrs766105286
SNPdbers766105286
MSV3drs766105286
GWAS Ctlgrs766105286
Max Magnitude0
ClinVar
Risk rs766105286(A;A)
Alt rs766105286(A;A)
Reference rs766105286(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000009.11:g.97873784G>A; NC_000009.11:g.97873784G>T
CLNSRC
CLNACC RCV000206783.1, RCV000205214.1,