rs1060499697

Orientation

plus

Stabilized

plus

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

Make rs1060499697(C;T)

Make rs1060499697(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

137234670

Gene

SLC34A3

is a	snp
is	mentioned by
dbSNP	rs1060499697
dbSNP (classic)	rs1060499697
ClinGen	rs1060499697
ebi	rs1060499697
HLI	rs1060499697
Exac	rs1060499697
Gnomad	rs1060499697
Varsome	rs1060499697
LitVar	rs1060499697
Map	rs1060499697
PheGenI	rs1060499697
Biobank	rs1060499697
1000 genomes	rs1060499697
hgdp	rs1060499697
ensembl	rs1060499697
geneview	rs1060499697
scholar	rs1060499697
google	rs1060499697
pharmgkb	rs1060499697
gwascentral	rs1060499697
openSNP	rs1060499697
23andMe	rs1060499697
SNPshot	rs1060499697
SNPdbe	rs1060499697
MSV3d	rs1060499697
GWAS Ctlg	rs1060499697

Max Magnitude

0

ClinVar
Risk	rs1060499697(T;T)
Alt	rs1060499697(T;T)
Reference	Rs1060499697(C;C)
Significance	Probable-Pathogenic
Disease	Autosomal recessive hypophosphatemic bone disease
Variation	info
Gene	SLC34A3
CLNDBN	Autosomal recessive hypophosphatemic bone disease
Reversed	0
HGVS	NC_000009.11:g.140129122C>T
CLNSRC
CLNACC	RCV000449572.1,