rs397507809

Orientation

plus

Stabilized

plus

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

Make rs397507809(ATCACCTTG;ATCACCTTG)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340198

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507809
dbSNP (classic)	rs397507809
ClinGen	rs397507809
ebi	rs397507809
HLI	rs397507809
Exac	rs397507809
Gnomad	rs397507809
Varsome	rs397507809
LitVar	rs397507809
Map	rs397507809
PheGenI	rs397507809
Biobank	rs397507809
1000 genomes	rs397507809
hgdp	rs397507809
ensembl	rs397507809
geneview	rs397507809
scholar	rs397507809
google	rs397507809
pharmgkb	rs397507809
gwascentral	rs397507809
openSNP	rs397507809
23andMe	rs397507809
SNPshot	rs397507809
SNPdbe	rs397507809
MSV3d	rs397507809
GWAS Ctlg	rs397507809

Max Magnitude

6

aka c.5835_5843dupATCACCTTG

ClinVar
Risk	rs397507809(ATCACCTTG;ATCACCTTG)
Alt	rs397507809(ATCACCTTG;ATCACCTTG)
Reference	Rs397507809(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914327_32914335dupATCACCTTG
CLNSRC	ClinVar
CLNACC	RCV000044769.2,