rs397507789

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;AAAAG)	6	Miscall in 23andMe v4 data; otherwise, BRCA2 variant considered pathogenic for breast cancer
(AAAAG;AAAAG)	0	common in clinvar

Make rs397507789(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339935

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507789
dbSNP (classic)	rs397507789
ClinGen	rs397507789
ebi	rs397507789
HLI	rs397507789
Exac	rs397507789
Gnomad	rs397507789
Varsome	rs397507789
LitVar	rs397507789
Map	rs397507789
PheGenI	rs397507789
Biobank	rs397507789
1000 genomes	rs397507789
hgdp	rs397507789
ensembl	rs397507789
geneview	rs397507789
scholar	rs397507789
google	rs397507789
pharmgkb	rs397507789
gwascentral	rs397507789
openSNP	rs397507789
23andMe	rs397507789
SNPshot	rs397507789
SNPdbe	rs397507789
MSV3d	rs397507789
GWAS Ctlg	rs397507789

Max Magnitude

6

aka c.5580_5584delAAAAG (p.Lys1860Asnfs)

23andMe name: i5009095

ClinVar
Risk	rs397507789(-;-)
Alt	rs397507789(-;-)
Reference	Rs397507789(AAAAG;AAAAG)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914072_32914076delAAAAG
CLNSRC	ClinVar
CLNACC	RCV000044686.2,