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rs730881710

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs730881710(-;-)
Make rs730881710(-;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95107211
GeneC9orf3, FANCC
is asnp
is mentioned by
dbSNPrs730881710
ebirs730881710
HLIrs730881710
Exacrs730881710
Varsomers730881710
Maprs730881710
PheGenIrs730881710
hapmaprs730881710
1000 genomesrs730881710
hgdprs730881710
ensemblrs730881710
gopubmedrs730881710
geneviewrs730881710
scholarrs730881710
googlers730881710
pharmgkbrs730881710
gwascentralrs730881710
openSNPrs730881710
23andMers730881710
23andMe allrs730881710
SNP Nexus

SNPshotrs730881710
SNPdbers730881710
MSV3drs730881710
GWAS Ctlgrs730881710
Max Magnitude0
ClinVar
Risk rs730881710(;)
Alt rs730881710(;)
Reference rs730881710(TC;TC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FANCC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.97869493_97869494delGA
CLNSRC
CLNACC RCV000160469.1,