rs746870368

Orientation

plus

Stabilized

plus

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

Make rs746870368(A;A)

Make rs746870368(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58696860

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs746870368
dbSNP (classic)	rs746870368
ClinGen	rs746870368
ebi	rs746870368
HLI	rs746870368
Exac	rs746870368
Gnomad	rs746870368
Varsome	rs746870368
LitVar	rs746870368
Map	rs746870368
PheGenI	rs746870368
Biobank	rs746870368
1000 genomes	rs746870368
hgdp	rs746870368
ensembl	rs746870368
geneview	rs746870368
scholar	rs746870368
google	rs746870368
pharmgkb	rs746870368
gwascentral	rs746870368
openSNP	rs746870368
23andMe	rs746870368
SNPshot	rs746870368
SNPdbe	rs746870368
MSV3d	rs746870368
GWAS Ctlg	rs746870368

Max Magnitude

0

ClinVar
Risk	rs746870368(A;A) rs746870368(T;T)
Alt	rs746870368(A;A) rs746870368(T;T)
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,