rs397507984

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;AT)	6	BRCA2 variant considered pathogenic for breast cancer
(AT;AT)	0	common in clinvar
(TA;TA)	0	common in clinvar

Make rs397507984(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32370485

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507984
dbSNP (classic)	rs397507984
ClinGen	rs397507984
ebi	rs397507984
HLI	rs397507984
Exac	rs397507984
Gnomad	rs397507984
Varsome	rs397507984
LitVar	rs397507984
Map	rs397507984
PheGenI	rs397507984
Biobank	rs397507984
1000 genomes	rs397507984
hgdp	rs397507984
ensembl	rs397507984
geneview	rs397507984
scholar	rs397507984
google	rs397507984
pharmgkb	rs397507984
gwascentral	rs397507984
openSNP	rs397507984
23andMe	rs397507984
SNPshot	rs397507984
SNPdbe	rs397507984
MSV3d	rs397507984
GWAS Ctlg	rs397507984

Max Magnitude

6

rs397507984 has merged into rs397507402

ClinVar
Risk	rs397507984(-;-)
Alt	rs397507984(-;-)
Reference	Rs397507984(TA;TA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32944622_32944623delAT
CLNSRC	ClinVar
CLNACC	RCV000045510.2,