rs876661338

Orientation

plus

Stabilized

plus

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

Make rs876661338(G;G)

Make rs876661338(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

177393763

Gene

SLC34A1

is a	snp
is	mentioned by
dbSNP	rs876661338
dbSNP (classic)	rs876661338
ClinGen	rs876661338
ebi	rs876661338
HLI	rs876661338
Exac	rs876661338
Gnomad	rs876661338
Varsome	rs876661338
LitVar	rs876661338
Map	rs876661338
PheGenI	rs876661338
Biobank	rs876661338
1000 genomes	rs876661338
hgdp	rs876661338
ensembl	rs876661338
geneview	rs876661338
scholar	rs876661338
google	rs876661338
pharmgkb	rs876661338
gwascentral	rs876661338
openSNP	rs876661338
23andMe	rs876661338
SNPshot	rs876661338
SNPdbe	rs876661338
MSV3d	rs876661338
GWAS Ctlg	rs876661338

Max Magnitude

0

ClinVar
Risk	rs876661338(G;G)
Alt	rs876661338(G;G)
Reference	Rs876661338(T;T)
Significance	Pathogenic
Disease	Hypercalcemia
Variation	info
Gene	SLC34A1
CLNDBN	Hypercalcemia, infantile, 2
Reversed	0
HGVS	NC_000005.9:g.176820764T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000223677.2,