rs121918234

Orientation

plus

Stabilized

plus

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

Make rs121918234(G;T)

Make rs121918234(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137234241

Gene

SLC34A3

is a	snp
is	mentioned by
dbSNP	rs121918234
dbSNP (classic)	rs121918234
ClinGen	rs121918234
ebi	rs121918234
HLI	rs121918234
Exac	rs121918234
Gnomad	rs121918234
Varsome	rs121918234
LitVar	rs121918234
Map	rs121918234
PheGenI	rs121918234
Biobank	rs121918234
1000 genomes	rs121918234
hgdp	rs121918234
ensembl	rs121918234
geneview	rs121918234
scholar	rs121918234
google	rs121918234
pharmgkb	rs121918234
gwascentral	rs121918234
openSNP	rs121918234
23andMe	rs121918234
SNPshot	rs121918234
SNPdbe	rs121918234
MSV3d	rs121918234
GWAS Ctlg	rs121918234

Max Magnitude

0

OMIM	609826
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121918234(A;A) rs121918234(C;C) rs121918234(T;T)
Alt	rs121918234(A;A) rs121918234(C;C) rs121918234(T;T)
Reference	Rs121918234(G;G)
Significance	Pathogenic
Disease	Autosomal recessive hypophosphatemic bone disease
Variation	info
Gene	SLC34A3
CLNDBN	Autosomal recessive hypophosphatemic bone disease
Reversed	0
HGVS	NC_000009.11:g.140128693G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001492.3,