rs145166656

Orientation

plus

Stabilized

plus

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

Make rs145166656(C;T)

Make rs145166656(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

47502992

Gene

PHKB

is a	snp
is	mentioned by
dbSNP	rs145166656
dbSNP (classic)	rs145166656
ClinGen	rs145166656
ebi	rs145166656
HLI	rs145166656
Exac	rs145166656
Gnomad	rs145166656
Varsome	rs145166656
LitVar	rs145166656
Map	rs145166656
PheGenI	rs145166656
Biobank	rs145166656
1000 genomes	rs145166656
hgdp	rs145166656
ensembl	rs145166656
geneview	rs145166656
scholar	rs145166656
google	rs145166656
pharmgkb	rs145166656
gwascentral	rs145166656
openSNP	rs145166656
23andMe	rs145166656
SNPshot	rs145166656
SNPdbe	rs145166656
MSV3d	rs145166656
GWAS Ctlg	rs145166656

Max Magnitude

0

ClinVar
Risk	rs145166656(T;T)
Alt	rs145166656(T;T)
Reference	Rs145166656(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHKB
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.47536903C>T
CLNSRC
CLNACC	RCV000489267.1,