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rs35910969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35910969(C;G)
Make rs35910969(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position74749174
GeneMIR3615, SLC9A3R1
is asnp
is mentioned by
dbSNPrs35910969
ebirs35910969
HLIrs35910969
Exacrs35910969
Varsomers35910969
Maprs35910969
PheGenIrs35910969
hapmaprs35910969
1000 genomesrs35910969
hgdprs35910969
ensemblrs35910969
gopubmedrs35910969
geneviewrs35910969
scholarrs35910969
googlers35910969
pharmgkbrs35910969
gwascentralrs35910969
openSNPrs35910969
23andMers35910969
23andMe allrs35910969
SNP Nexus

SNPshotrs35910969
SNPdbers35910969
MSV3drs35910969
GWAS Ctlgrs35910969
GMAF0.01194
Max Magnitude0
OMIM604990
Desc
Variant0001
Relatedalso


ClinVar
Risk rs35910969(G;G)
Alt rs35910969(G;G)
Reference rs35910969(C;C)
Significance Pathogenic
Disease Nephrolithiasis/osteoporosis
Variation info
Gene MIR3615 SLC9A3R1
CLNDBN Nephrolithiasis/osteoporosis, hypophosphatemic, 2
Reversed 0
HGVS NC_000017.10:g.72745313C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005588.2,