rs730881635

Orientation

minus

Stabilized

minus

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

Make rs730881635(A;T)

Make rs730881635(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

61799284

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs730881635
dbSNP (classic)	rs730881635
ClinGen	rs730881635
ebi	rs730881635
HLI	rs730881635
Exac	rs730881635
Gnomad	rs730881635
Varsome	rs730881635
LitVar	rs730881635
Map	rs730881635
PheGenI	rs730881635
Biobank	rs730881635
1000 genomes	rs730881635
hgdp	rs730881635
ensembl	rs730881635
geneview	rs730881635
scholar	rs730881635
google	rs730881635
pharmgkb	rs730881635
gwascentral	rs730881635
openSNP	rs730881635
23andMe	rs730881635
SNPshot	rs730881635
SNPdbe	rs730881635
MSV3d	rs730881635
GWAS Ctlg	rs730881635

Max Magnitude

0

ClinVar
Risk	rs730881635(T;T)
Alt	rs730881635(T;T)
Reference	Rs730881635(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.59876645T>A
CLNSRC
CLNACC	RCV000160337.1,