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rs753885687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753885687(C;G)
Make rs753885687(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95107065
GeneC9orf3, FANCC, LOC107987102
is asnp
is mentioned by
dbSNPrs753885687
dbSNP (classic)rs753885687
ClinGenrs753885687
ebirs753885687
HLIrs753885687
Exacrs753885687
Gnomadrs753885687
Varsomers753885687
LitVarrs753885687
Maprs753885687
PheGenIrs753885687
Biobankrs753885687
1000 genomesrs753885687
hgdprs753885687
ensemblrs753885687
geneviewrs753885687
scholarrs753885687
googlers753885687
pharmgkbrs753885687
gwascentralrs753885687
openSNPrs753885687
23andMers753885687
23andMe allrs753885687
SNPshotrs753885687
SNPdbers753885687
MSV3drs753885687
GWAS Ctlgrs753885687
Max Magnitude0
ClinVar
Risk rs753885687(G;G)
Alt rs753885687(G;G)
Reference Rs753885687(C;C)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 0
HGVS NC_000009.11:g.97869347C>G
CLNSRC
CLNACC RCV000409707.1,