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

rs730881708

From SNPedia

Orientationminus
Geno Mag Summary
(GAGA;GAGA) 0 common in clinvar
Make rs730881708(-;-)
Make rs730881708(-;GAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position95171110
GeneFANCC
is asnp
is mentioned by
dbSNPrs730881708
ebirs730881708
HLIrs730881708
Exacrs730881708
Varsomers730881708
Maprs730881708
PheGenIrs730881708
hapmaprs730881708
1000 genomesrs730881708
hgdprs730881708
ensemblrs730881708
gopubmedrs730881708
geneviewrs730881708
scholarrs730881708
googlers730881708
pharmgkbrs730881708
gwascentralrs730881708
openSNPrs730881708
23andMers730881708
23andMe allrs730881708
SNP Nexus

SNPshotrs730881708
SNPdbers730881708
MSV3drs730881708
GWAS Ctlgrs730881708
Max Magnitude0
ClinVar
Risk rs730881708(;)
Alt rs730881708(;)
Reference rs730881708(GAGA;GAGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FANCC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.97933392_97933395delTCTC
CLNSRC
CLNACC RCV000160466.1,