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rs1057516420

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516420(C;T)
Make rs1057516420(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95111483
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs1057516420
dbSNP (classic)rs1057516420
ClinGenrs1057516420
ebirs1057516420
HLIrs1057516420
Exacrs1057516420
Gnomadrs1057516420
Varsomers1057516420
LitVarrs1057516420
Maprs1057516420
PheGenIrs1057516420
Biobankrs1057516420
1000 genomesrs1057516420
hgdprs1057516420
ensemblrs1057516420
geneviewrs1057516420
scholarrs1057516420
googlers1057516420
pharmgkbrs1057516420
gwascentralrs1057516420
openSNPrs1057516420
23andMers1057516420
23andMe allrs1057516420
SNPshotrs1057516420
SNPdbers1057516420
MSV3drs1057516420
GWAS Ctlgrs1057516420
Max Magnitude0
ClinVar
Risk rs1057516420(T;T)
Alt rs1057516420(T;T)
Reference Rs1057516420(C;C)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97873765G>A
CLNSRC
CLNACC RCV000411906.1,