rs1060502356

Orientation

minus

Stabilized

minus

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

Make rs1060502356(-;-)

Make rs1060502356(-;GTAAAG)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

43057046

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs1060502356
dbSNP (classic)	rs1060502356
ClinGen	rs1060502356
ebi	rs1060502356
HLI	rs1060502356
Exac	rs1060502356
Gnomad	rs1060502356
Varsome	rs1060502356
LitVar	rs1060502356
Map	rs1060502356
PheGenI	rs1060502356
Biobank	rs1060502356
1000 genomes	rs1060502356
hgdp	rs1060502356
ensembl	rs1060502356
geneview	rs1060502356
scholar	rs1060502356
google	rs1060502356
pharmgkb	rs1060502356
gwascentral	rs1060502356
openSNP	rs1060502356
23andMe	rs1060502356
SNPshot	rs1060502356
SNPdbe	rs1060502356
MSV3d	rs1060502356
GWAS Ctlg	rs1060502356

Max Magnitude

0

ClinVar
Risk	rs1060502356(-;-)
Alt	rs1060502356(-;-)
Reference	Rs1060502356(GTAAAG;GTAAAG)
Significance	Probable-Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.41209063_41209068delCTTTAC
CLNSRC
CLNACC	RCV000463038.1,