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rs119486097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs119486097(A;A)
Make rs119486097(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position74763436
GeneSLC9A3R1
is asnp
is mentioned by
dbSNPrs119486097
ebirs119486097
HLIrs119486097
Exacrs119486097
Varsomers119486097
Maprs119486097
PheGenIrs119486097
hapmaprs119486097
1000 genomesrs119486097
hgdprs119486097
ensemblrs119486097
gopubmedrs119486097
geneviewrs119486097
scholarrs119486097
googlers119486097
pharmgkbrs119486097
gwascentralrs119486097
openSNPrs119486097
23andMers119486097
23andMe allrs119486097
SNP Nexus

SNPshotrs119486097
SNPdbers119486097
MSV3drs119486097
GWAS Ctlgrs119486097
GMAF0.001837
Max Magnitude0
OMIM604990
Desc
Variant0003
Relatedalso
ClinVar
Risk rs119486097(A;A)
Alt rs119486097(A;A)
Reference rs119486097(G;G)
Significance Pathogenic
Disease Nephrolithiasis/osteoporosis
Variation info
Gene SLC9A3R1
CLNDBN Nephrolithiasis/osteoporosis, hypophosphatemic, 2
Reversed 0
HGVS NC_000017.10:g.72759575G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005590.2,