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rs746870368

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746870368(A;A)
Make rs746870368(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58696860
GeneRAD51C
is asnp
is mentioned by
dbSNPrs746870368
ebirs746870368
HLIrs746870368
Exacrs746870368
Varsomers746870368
Maprs746870368
PheGenIrs746870368
hapmaprs746870368
1000 genomesrs746870368
hgdprs746870368
ensemblrs746870368
gopubmedrs746870368
geneviewrs746870368
scholarrs746870368
googlers746870368
pharmgkbrs746870368
gwascentralrs746870368
openSNPrs746870368
23andMers746870368
23andMe allrs746870368
SNP Nexus

SNPshotrs746870368
SNPdbers746870368
MSV3drs746870368
GWAS Ctlgrs746870368
Max Magnitude0
ClinVar
Risk rs746870368(A;A)
Alt rs746870368(A;A)
Reference rs746870368(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAD51C
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.56774221G>T
CLNSRC
CLNACC RCV000236630.1,