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rs730881940

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881940(-;-)
Make rs730881940(-;A)
Make rs730881940(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58695179
GeneRAD51C
is asnp
is mentioned by
dbSNPrs730881940
ebirs730881940
HLIrs730881940
Exacrs730881940
Varsomers730881940
Maprs730881940
PheGenIrs730881940
hapmaprs730881940
1000 genomesrs730881940
hgdprs730881940
ensemblrs730881940
gopubmedrs730881940
geneviewrs730881940
scholarrs730881940
googlers730881940
pharmgkbrs730881940
gwascentralrs730881940
openSNPrs730881940
23andMers730881940
23andMe allrs730881940
SNP Nexus

SNPshotrs730881940
SNPdbers730881940
MSV3drs730881940
GWAS Ctlgrs730881940
Max Magnitude0
ClinVar
Risk rs730881940(A;A)
Alt rs730881940(A;A)
Reference rs730881940(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56772540dupA
CLNSRC
CLNACC RCV000160934.1,