rs878855150

Orientation

minus

Stabilized

minus

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

Make rs878855150(-;CAAA)

Make rs878855150(CAAA;CAAA)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

61684052

Gene

BRIP1

is a	snp
is	mentioned by
dbSNP	rs878855150
dbSNP (classic)	rs878855150
ClinGen	rs878855150
ebi	rs878855150
HLI	rs878855150
Exac	rs878855150
Gnomad	rs878855150
Varsome	rs878855150
LitVar	rs878855150
Map	rs878855150
PheGenI	rs878855150
Biobank	rs878855150
1000 genomes	rs878855150
hgdp	rs878855150
ensembl	rs878855150
geneview	rs878855150
scholar	rs878855150
google	rs878855150
pharmgkb	rs878855150
gwascentral	rs878855150
openSNP	rs878855150
23andMe	rs878855150
SNPshot	rs878855150
SNPdbe	rs878855150
MSV3d	rs878855150
GWAS Ctlg	rs878855150

Max Magnitude

0

ClinVar
Risk	rs878855150(CAAA;CAAA)
Alt	rs878855150(CAAA;CAAA)
Reference	Rs878855150(-;-)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast Fanconi anemia
Variation	info
Gene	BRIP1
CLNDBN	Familial cancer of breast Fanconi anemia, complementation group J
Reversed	1
HGVS	NC_000017.10:g.59761414_59761417dupTTTG
CLNSRC
CLNACC	RCV000233395.1,