rs149364097

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	6	Ovarian cancer susceptibility

Make rs149364097(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

61801348

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs149364097
dbSNP (classic)	rs149364097
ClinGen	rs149364097
ebi	rs149364097
HLI	rs149364097
Exac	rs149364097
Gnomad	rs149364097
Varsome	rs149364097
LitVar	rs149364097
Map	rs149364097
PheGenI	rs149364097
Biobank	rs149364097
1000 genomes	rs149364097
hgdp	rs149364097
ensembl	rs149364097
geneview	rs149364097
scholar	rs149364097
google	rs149364097
pharmgkb	rs149364097
gwascentral	rs149364097
openSNP	rs149364097
23andMe	rs149364097
SNPshot	rs149364097
SNPdbe	rs149364097
MSV3d	rs149364097
GWAS Ctlg	rs149364097

Max Magnitude

6

ClinVar
Risk	rs149364097(A;A) rs149364097(G;G) rs149364097(T;T)
Alt	rs149364097(A;A) rs149364097(G;G) rs149364097(T;T)
Reference	Rs149364097(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not specified not provided Familial cancer of breast
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group J not specified not provided Familial cancer of breast
Reversed	0
HGVS	NC_000017.10:g.59878709C>A; NC_000017.10:g.59878709C>G; NC_000017.10:g.59878709C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000213526.1, RCV000023492.2, RCV000120412.1, RCV000131544.3, RCV000216316.2, RCV000466014.1, RCV000431413.1,