rs772486760

Orientation

plus

Stabilized

plus

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

Make rs772486760(-;TTTC)

Make rs772486760(TTTC;TTTC)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

214781413

Gene

BARD1

is a	snp
is	mentioned by
dbSNP	rs772486760
dbSNP (classic)	rs772486760
ClinGen	rs772486760
ebi	rs772486760
HLI	rs772486760
Exac	rs772486760
Gnomad	rs772486760
Varsome	rs772486760
LitVar	rs772486760
Map	rs772486760
PheGenI	rs772486760
Biobank	rs772486760
1000 genomes	rs772486760
hgdp	rs772486760
ensembl	rs772486760
geneview	rs772486760
scholar	rs772486760
google	rs772486760
pharmgkb	rs772486760
gwascentral	rs772486760
openSNP	rs772486760
23andMe	rs772486760
SNPshot	rs772486760
SNPdbe	rs772486760
MSV3d	rs772486760
GWAS Ctlg	rs772486760

Max Magnitude

0

ClinVar
Risk	rs772486760(CTTT;CTTT)
Alt	rs772486760(CTTT;CTTT)
Reference	Rs772486760(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BARD1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.215646138_215646141dupCTTT
CLNSRC
CLNACC	RCV000220804.1,