rs374435098

Orientation

plus

Stabilized

plus

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

Make rs374435098(C;T)

Make rs374435098(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43079400

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs374435098
dbSNP (classic)	rs374435098
ClinGen	rs374435098
ebi	rs374435098
HLI	rs374435098
Exac	rs374435098
Gnomad	rs374435098
Varsome	rs374435098
LitVar	rs374435098
Map	rs374435098
PheGenI	rs374435098
Biobank	rs374435098
1000 genomes	rs374435098
hgdp	rs374435098
ensembl	rs374435098
geneview	rs374435098
scholar	rs374435098
google	rs374435098
pharmgkb	rs374435098
gwascentral	rs374435098
openSNP	rs374435098
23andMe	rs374435098
SNPshot	rs374435098
SNPdbe	rs374435098
MSV3d	rs374435098
GWAS Ctlg	rs374435098

Max Magnitude

0

ClinVar
Risk	rs374435098(T;T)
Alt	rs374435098(T;T)
Reference	Rs374435098(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000017.10:g.41231417C>T
CLNSRC
CLNACC	RCV000149888.2,