rs121918372

Orientation

minus

Stabilized

minus

Make rs121918372(A;A)

Make rs121918372(A;G)

Make rs121918372(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

49409410

Gene

PHB

is a	snp
is	mentioned by
dbSNP	rs121918372
dbSNP (classic)	rs121918372
ClinGen	rs121918372
ebi	rs121918372
HLI	rs121918372
Exac	rs121918372
Gnomad	rs121918372
Varsome	rs121918372
LitVar	rs121918372
Map	rs121918372
PheGenI	rs121918372
Biobank	rs121918372
1000 genomes	rs121918372
hgdp	rs121918372
ensembl	rs121918372
geneview	rs121918372
scholar	rs121918372
google	rs121918372
pharmgkb	rs121918372
gwascentral	rs121918372
openSNP	rs121918372
23andMe	rs121918372
SNPshot	rs121918372
SNPdbe	rs121918372
MSV3d	rs121918372
GWAS Ctlg	rs121918372

Max Magnitude

0

OMIM	176705
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918372(A;A)
Alt	rs121918372(A;A)
Reference	rs121918372(G;G)
Significance	Other
Disease	Breast cancer
Variation	info
Gene	PHB
CLNDBN	Breast cancer, susceptibility to
Reversed	1
HGVS	NC_000017.10:g.47486772C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014325.1,