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rs1057517203

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517203(-;A)
Make rs1057517203(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95149968
GeneFANCC
is asnp
is mentioned by
dbSNPrs1057517203
dbSNP (old)rs1057517203
ClinGenrs1057517203
ebirs1057517203
HLIrs1057517203
Exacrs1057517203
Gnomadrs1057517203
Varsomers1057517203
Maprs1057517203
PheGenIrs1057517203
Biobankrs1057517203
1000 genomesrs1057517203
hgdprs1057517203
ensemblrs1057517203
gopubmedrs1057517203
geneviewrs1057517203
scholarrs1057517203
googlers1057517203
pharmgkbrs1057517203
gwascentralrs1057517203
openSNPrs1057517203
23andMers1057517203
23andMe allrs1057517203
SNPshotrs1057517203
SNPdbers1057517203
MSV3drs1057517203
GWAS Ctlgrs1057517203
Max Magnitude0
ClinVar
Risk rs1057517203(A;A)
Alt rs1057517203(A;A)
Reference Rs1057517203(-;-)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCC
CLNDBN Fanconi anemia, complementation group C
Reversed 1
HGVS NC_000009.11:g.97912251dupT
CLNSRC
CLNACC RCV000409673.1,