rs28903098

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0

Make rs28903098(C;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

61859862

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs28903098
dbSNP (classic)	rs28903098
ClinGen	rs28903098
ebi	rs28903098
HLI	rs28903098
Exac	rs28903098
Gnomad	rs28903098
Varsome	rs28903098
LitVar	rs28903098
Map	rs28903098
PheGenI	rs28903098
Biobank	rs28903098
1000 genomes	rs28903098
hgdp	rs28903098
ensembl	rs28903098
geneview	rs28903098
scholar	rs28903098
google	rs28903098
pharmgkb	rs28903098
gwascentral	rs28903098
openSNP	rs28903098
23andMe	rs28903098
SNPshot	rs28903098
SNPdbe	rs28903098
MSV3d	rs28903098
GWAS Ctlg	rs28903098

Merged from

Rs137852984

Max Magnitude

0

OMIM	605882
Desc	BREAST CANCER, EARLY-ONSET
Variant	0001
Related	also

ClinVar
Risk	rs28903098(A;A) Rs28903098(G;G)
Alt	rs28903098(A;A) Rs28903098(G;G)
Reference	Rs28903098(C;C)
Significance	Pathogenic
Disease	Breast cancer Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not specified Neoplasm of ovary not provided
Variation	info
Gene	BRIP1
CLNDBN	Breast cancer, early-onset Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not specified Neoplasm of ovary not provided
Reversed	1
HGVS	NC_000017.10:g.59937223G>C; NC_000017.10:g.59937223G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005002.2, RCV000116124.7, RCV000199377.4, RCV000200979.4, RCV000409748.1, RCV000410864.1, RCV000160330.2, RCV000216538.1,