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rs730881933

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881933(A;A)
Make rs730881933(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58724101
GeneLOC105371843, RAD51C
is asnp
is mentioned by
dbSNPrs730881933
ebirs730881933
HLIrs730881933
Exacrs730881933
Varsomers730881933
Maprs730881933
PheGenIrs730881933
hapmaprs730881933
1000 genomesrs730881933
hgdprs730881933
ensemblrs730881933
gopubmedrs730881933
geneviewrs730881933
scholarrs730881933
googlers730881933
pharmgkbrs730881933
gwascentralrs730881933
openSNPrs730881933
23andMers730881933
23andMe allrs730881933
SNP Nexus

SNPshotrs730881933
SNPdbers730881933
MSV3drs730881933
GWAS Ctlgrs730881933
Max Magnitude0
ClinVar
Risk rs730881933(A;A)
Alt rs730881933(A;A)
Reference rs730881933(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAD51C
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.56801462G>A
CLNSRC
CLNACC RCV000160926.2,