rs206118

Orientation

minus

Stabilized

minus

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

Make rs206118(C;C)

Make rs206118(C;T)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32315655

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs206118
dbSNP (classic)	rs206118
ClinGen	rs206118
ebi	rs206118
HLI	rs206118
Exac	rs206118
Gnomad	rs206118
Varsome	rs206118
LitVar	rs206118
Map	rs206118
PheGenI	rs206118
Biobank	rs206118
1000 genomes	rs206118
hgdp	rs206118
ensembl	rs206118
geneview	rs206118
scholar	rs206118
google	rs206118
pharmgkb	rs206118
gwascentral	rs206118
openSNP	rs206118
23andMe	rs206118
SNPshot	rs206118
SNPdbe	rs206118
MSV3d	rs206118
GWAS Ctlg	rs206118

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 25243787] Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival

ClinVar
Risk	rs206118(C;C)
Alt	rs206118(C;C)
Reference	Rs206118(T;T)
Significance	Non-pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Fanconi anemia
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Fanconi anemia
Reversed	1
HGVS	NC_000013.10:g.32889792A>G
CLNSRC
CLNACC	RCV000191546.1, RCV000297492.1, RCV000338379.1,