rs1057517643

Orientation

minus

Stabilized

minus

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

Make rs1057517643(A;A)

Make rs1057517643(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

61744578

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs1057517643
dbSNP (classic)	rs1057517643
ClinGen	rs1057517643
ebi	rs1057517643
HLI	rs1057517643
Exac	rs1057517643
Gnomad	rs1057517643
Varsome	rs1057517643
LitVar	rs1057517643
Map	rs1057517643
PheGenI	rs1057517643
Biobank	rs1057517643
1000 genomes	rs1057517643
hgdp	rs1057517643
ensembl	rs1057517643
geneview	rs1057517643
scholar	rs1057517643
google	rs1057517643
pharmgkb	rs1057517643
gwascentral	rs1057517643
openSNP	rs1057517643
23andMe	rs1057517643
SNPshot	rs1057517643
SNPdbe	rs1057517643
MSV3d	rs1057517643
GWAS Ctlg	rs1057517643

Max Magnitude

0

ClinVar
Risk	rs1057517643(A;A)
Alt	rs1057517643(A;A)
Reference	Rs1057517643(T;T)
Significance	Probable-Pathogenic
Disease	Neoplasm of ovary Fanconi anemia
Variation	info
Gene	BRIP1
CLNDBN	Neoplasm of ovary Fanconi anemia, complementation group J
Reversed	1
HGVS	NC_000017.10:g.59821939A>T
CLNSRC
CLNACC	RCV000409317.1, RCV000411722.1,