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

rs1057517125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517125(G;T)
Make rs1057517125(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95149922
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057517125
dbSNP (classic)rs1057517125
ClinGenrs1057517125
ebirs1057517125
HLIrs1057517125
Exacrs1057517125
Gnomadrs1057517125
Varsomers1057517125
LitVarrs1057517125
Maprs1057517125
PheGenIrs1057517125
Biobankrs1057517125
1000 genomesrs1057517125
hgdprs1057517125
ensemblrs1057517125
geneviewrs1057517125
scholarrs1057517125
googlers1057517125
pharmgkbrs1057517125
gwascentralrs1057517125
openSNPrs1057517125
23andMers1057517125
23andMe allrs1057517125
SNPshotrs1057517125
SNPdbers1057517125
MSV3drs1057517125
GWAS Ctlgrs1057517125
Max Magnitude0
ClinVar
Risk rs1057517125(T;T)
Alt rs1057517125(T;T)
Reference Rs1057517125(G;G)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97912204C>A
CLNSRC
CLNACC RCV000409465.1,