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rs730881941

From SNPedia

Orientationplus
Geno Mag Summary
(CAGGG;CAGGG) 0 common in clinvar
Make rs730881941(-;-)
Make rs730881941(-;CAGGG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58724037
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs730881941
ebirs730881941
HLIrs730881941
Exacrs730881941
Varsomers730881941
Maprs730881941
PheGenIrs730881941
hapmaprs730881941
1000 genomesrs730881941
hgdprs730881941
ensemblrs730881941
gopubmedrs730881941
geneviewrs730881941
scholarrs730881941
googlers730881941
pharmgkbrs730881941
gwascentralrs730881941
openSNPrs730881941
23andMers730881941
23andMe allrs730881941
SNP Nexus

SNPshotrs730881941
SNPdbers730881941
MSV3drs730881941
GWAS Ctlgrs730881941
Max Magnitude0
ClinVar
Risk rs730881941(;)
Alt rs730881941(;)
Reference rs730881941(CAGGG;CAGGG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.56801398_56801402delCAGGG
CLNSRC
CLNACC RCV000160935.1,