rs1057518635

Orientation

plus

Stabilized

plus

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

Make rs1057518635(-;-)

Make rs1057518635(-;ATAG)

Make rs1057518635(ATAG;ATAG)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32340369

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1057518635
dbSNP (classic)	rs1057518635
ClinGen	rs1057518635
ebi	rs1057518635
HLI	rs1057518635
Exac	rs1057518635
Gnomad	rs1057518635
Varsome	rs1057518635
LitVar	rs1057518635
Map	rs1057518635
PheGenI	rs1057518635
Biobank	rs1057518635
1000 genomes	rs1057518635
hgdp	rs1057518635
ensembl	rs1057518635
geneview	rs1057518635
scholar	rs1057518635
google	rs1057518635
pharmgkb	rs1057518635
gwascentral	rs1057518635
openSNP	rs1057518635
23andMe	rs1057518635
SNPshot	rs1057518635
SNPdbe	rs1057518635
MSV3d	rs1057518635
GWAS Ctlg	rs1057518635

Max Magnitude

0

ClinVar
Risk	rs1057518635(-;-)
Alt	rs1057518635(-;-)
Reference	Rs1057518635(AGAT;AGAT)
Significance	Pathogenic
Disease	Neoplasm of breast not provided
Variation	info
Gene	BRCA2
CLNDBN	Neoplasm of breast not provided
Reversed	0
HGVS	NC_000013.10:g.32914506_32914509delATAG
CLNSRC
CLNACC	RCV000414026.1, RCV000479529.1,