rs1057521184

Orientation

plus

Stabilized

plus

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

Make rs1057521184(G;T)

Make rs1057521184(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32363372

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1057521184
dbSNP (classic)	rs1057521184
ClinGen	rs1057521184
ebi	rs1057521184
HLI	rs1057521184
Exac	rs1057521184
Gnomad	rs1057521184
Varsome	rs1057521184
LitVar	rs1057521184
Map	rs1057521184
PheGenI	rs1057521184
Biobank	rs1057521184
1000 genomes	rs1057521184
hgdp	rs1057521184
ensembl	rs1057521184
geneview	rs1057521184
scholar	rs1057521184
google	rs1057521184
pharmgkb	rs1057521184
gwascentral	rs1057521184
openSNP	rs1057521184
23andMe	rs1057521184
SNPshot	rs1057521184
SNPdbe	rs1057521184
MSV3d	rs1057521184
GWAS Ctlg	rs1057521184

Max Magnitude

0

ClinVar
Risk	rs1057521184(T;T)
Alt	rs1057521184(T;T)
Reference	Rs1057521184(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	BRCA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.32937509G>T
CLNSRC
CLNACC	RCV000417977.1,