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

rs759900071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759900071(A;A)
Make rs759900071(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95117318
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs759900071
dbSNP (classic)rs759900071
ClinGenrs759900071
ebirs759900071
HLIrs759900071
Exacrs759900071
Gnomadrs759900071
Varsomers759900071
LitVarrs759900071
Maprs759900071
PheGenIrs759900071
Biobankrs759900071
1000 genomesrs759900071
hgdprs759900071
ensemblrs759900071
geneviewrs759900071
scholarrs759900071
googlers759900071
pharmgkbrs759900071
gwascentralrs759900071
openSNPrs759900071
23andMers759900071
23andMe allrs759900071
SNPshotrs759900071
SNPdbers759900071
MSV3drs759900071
GWAS Ctlgrs759900071
Max Magnitude0
ClinVar
Risk rs759900071(A;A) rs759900071(C;C)
Alt rs759900071(A;A) rs759900071(C;C)
Reference Rs759900071(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FANCC
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.97879600G>A
CLNSRC
CLNACC RCV000483955.1,