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rs876661338

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661338(G;G)
Make rs876661338(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position177393763
GeneSLC34A1
is asnp
is mentioned by
dbSNPrs876661338
ebirs876661338
HLIrs876661338
Exacrs876661338
Varsomers876661338
Maprs876661338
PheGenIrs876661338
hapmaprs876661338
1000 genomesrs876661338
hgdprs876661338
ensemblrs876661338
gopubmedrs876661338
geneviewrs876661338
scholarrs876661338
googlers876661338
pharmgkbrs876661338
gwascentralrs876661338
openSNPrs876661338
23andMers876661338
23andMe allrs876661338
SNP Nexus

SNPshotrs876661338
SNPdbers876661338
MSV3drs876661338
GWAS Ctlgrs876661338
Max Magnitude0
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 RCV000223677.1,