rs794729659

Orientation

plus

Stabilized

plus

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

Make rs794729659(-;-)

Make rs794729659(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

137232627

Gene

SLC34A3

is a	snp
is	mentioned by
dbSNP	rs794729659
dbSNP (classic)	rs794729659
ClinGen	rs794729659
ebi	rs794729659
HLI	rs794729659
Exac	rs794729659
Gnomad	rs794729659
Varsome	rs794729659
LitVar	rs794729659
Map	rs794729659
PheGenI	rs794729659
Biobank	rs794729659
1000 genomes	rs794729659
hgdp	rs794729659
ensembl	rs794729659
geneview	rs794729659
scholar	rs794729659
google	rs794729659
pharmgkb	rs794729659
gwascentral	rs794729659
openSNP	rs794729659
23andMe	rs794729659
SNPshot	rs794729659
SNPdbe	rs794729659
MSV3d	rs794729659
GWAS Ctlg	rs794729659

Max Magnitude

0

ClinVar
Risk	rs794729659(-;-)
Alt	rs794729659(-;-)
Reference	Rs794729659(C;C)
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.140127079delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001495.3,