rs397507851

Orientation

plus

Stabilized

plus

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

Make rs397507851(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340763

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507851
dbSNP (classic)	rs397507851
ClinGen	rs397507851
ebi	rs397507851
HLI	rs397507851
Exac	rs397507851
Gnomad	rs397507851
Varsome	rs397507851
LitVar	rs397507851
Map	rs397507851
PheGenI	rs397507851
Biobank	rs397507851
1000 genomes	rs397507851
hgdp	rs397507851
ensembl	rs397507851
geneview	rs397507851
scholar	rs397507851
google	rs397507851
pharmgkb	rs397507851
gwascentral	rs397507851
openSNP	rs397507851
23andMe	rs397507851
SNPshot	rs397507851
SNPdbe	rs397507851
MSV3d	rs397507851
GWAS Ctlg	rs397507851

Max Magnitude

6

ClinVar
Risk	rs397507851(-;-)
Alt	rs397507851(-;-)
Reference	Rs397507851(TTAAATG;TTAAATG)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914900_32914906delAAATGTT
CLNSRC	ClinVar
CLNACC	RCV000044937.2, RCV000166653.2, RCV000241449.2,