rs61757642

Orientation

plus

Stabilized

plus

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

Make rs61757642(A;T)

Make rs61757642(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394936

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs61757642
dbSNP (classic)	rs61757642
ClinGen	rs61757642
ebi	rs61757642
HLI	rs61757642
Exac	rs61757642
Gnomad	rs61757642
Varsome	rs61757642
LitVar	rs61757642
Map	rs61757642
PheGenI	rs61757642
Biobank	rs61757642
1000 genomes	rs61757642
hgdp	rs61757642
ensembl	rs61757642
geneview	rs61757642
scholar	rs61757642
google	rs61757642
pharmgkb	rs61757642
gwascentral	rs61757642
openSNP	rs61757642
23andMe	rs61757642
SNPshot	rs61757642
SNPdbe	rs61757642
MSV3d	rs61757642
GWAS Ctlg	rs61757642

Max Magnitude

0

ClinVar
Risk	rs61757642(T;T)
Alt	rs61757642(T;T)
Reference	Rs61757642(A;A)
Significance	Other
Disease	Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32969073A>T
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031825.7, RCV000045838.7, RCV000131261.3, RCV000167798.5,