rs786203384

Orientation

minus

Stabilized

minus

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

Make rs786203384(A;TCC)

Make rs786203384(TCC;TCC)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

61744581

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs786203384
dbSNP (classic)	rs786203384
ClinGen	rs786203384
ebi	rs786203384
HLI	rs786203384
Exac	rs786203384
Gnomad	rs786203384
Varsome	rs786203384
LitVar	rs786203384
Map	rs786203384
PheGenI	rs786203384
Biobank	rs786203384
1000 genomes	rs786203384
hgdp	rs786203384
ensembl	rs786203384
geneview	rs786203384
scholar	rs786203384
google	rs786203384
pharmgkb	rs786203384
gwascentral	rs786203384
openSNP	rs786203384
23andMe	rs786203384
SNPshot	rs786203384
SNPdbe	rs786203384
MSV3d	rs786203384
GWAS Ctlg	rs786203384

Max Magnitude

0

ClinVar
Risk	rs786203384(TCC;TCC)
Alt	rs786203384(TCC;TCC)
Reference	Rs786203384(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia not provided
Variation	info
Gene	BRIP1
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast Fanconi anemia, complementation group J not provided
Reversed	1
HGVS	NC_000017.10:g.59821942delTinsGGA
CLNSRC
CLNACC	RCV000166665.2, RCV000203877.2, RCV000485974.1,