rs730881933

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs730881933(A;A)

Make rs730881933(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58724101

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs730881933
dbSNP (classic)	rs730881933
ClinGen	rs730881933
ebi	rs730881933
HLI	rs730881933
Exac	rs730881933
Gnomad	rs730881933
Varsome	rs730881933
LitVar	rs730881933
Map	rs730881933
PheGenI	rs730881933
Biobank	rs730881933
1000 genomes	rs730881933
hgdp	rs730881933
ensembl	rs730881933
geneview	rs730881933
scholar	rs730881933
google	rs730881933
pharmgkb	rs730881933
gwascentral	rs730881933
openSNP	rs730881933
23andMe	rs730881933
SNPshot	rs730881933
SNPdbe	rs730881933
MSV3d	rs730881933
GWAS Ctlg	rs730881933

Max Magnitude

0

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,