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rs1057516455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516455(A;A)
Make rs1057516455(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95101785
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs1057516455
dbSNP (old)rs1057516455
ClinGenrs1057516455
ebirs1057516455
HLIrs1057516455
Exacrs1057516455
Gnomadrs1057516455
Varsomers1057516455
LitVarrs1057516455
Maprs1057516455
PheGenIrs1057516455
Biobankrs1057516455
1000 genomesrs1057516455
hgdprs1057516455
ensemblrs1057516455
gopubmedrs1057516455
geneviewrs1057516455
scholarrs1057516455
googlers1057516455
pharmgkbrs1057516455
gwascentralrs1057516455
openSNPrs1057516455
23andMers1057516455
23andMe allrs1057516455
SNPshotrs1057516455
SNPdbers1057516455
MSV3drs1057516455
GWAS Ctlgrs1057516455
Max Magnitude0
ClinVar
Risk rs1057516455(A;A)
Alt rs1057516455(A;A)
Reference Rs1057516455(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.97864067C>T
CLNSRC
CLNACC RCV000411700.1,