rs1057518637

Orientation

plus

Stabilized

plus

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

Make rs1057518637(C;T)

Make rs1057518637(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32336621

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1057518637
dbSNP (classic)	rs1057518637
ClinGen	rs1057518637
ebi	rs1057518637
HLI	rs1057518637
Exac	rs1057518637
Gnomad	rs1057518637
Varsome	rs1057518637
LitVar	rs1057518637
Map	rs1057518637
PheGenI	rs1057518637
Biobank	rs1057518637
1000 genomes	rs1057518637
hgdp	rs1057518637
ensembl	rs1057518637
geneview	rs1057518637
scholar	rs1057518637
google	rs1057518637
pharmgkb	rs1057518637
gwascentral	rs1057518637
openSNP	rs1057518637
23andMe	rs1057518637
SNPshot	rs1057518637
SNPdbe	rs1057518637
MSV3d	rs1057518637
GWAS Ctlg	rs1057518637

Max Magnitude

0

ClinVar
Risk	rs1057518637(T;T)
Alt	rs1057518637(T;T)
Reference	Rs1057518637(C;C)
Significance	Pathogenic
Disease	Neoplasm of breast
Variation	info
Gene	BRCA2
CLNDBN	Neoplasm of breast
Reversed	0
HGVS	NC_000013.10:g.32910758C>T
CLNSRC
CLNACC	RCV000414647.1,