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rs137853141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853141(C;T)
Make rs137853141(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position25662818
GeneSLC34A2
is asnp
is mentioned by
dbSNPrs137853141
ebirs137853141
HLIrs137853141
Exacrs137853141
Varsomers137853141
Maprs137853141
PheGenIrs137853141
hapmaprs137853141
1000 genomesrs137853141
hgdprs137853141
ensemblrs137853141
gopubmedrs137853141
geneviewrs137853141
scholarrs137853141
googlers137853141
pharmgkbrs137853141
gwascentralrs137853141
openSNPrs137853141
23andMers137853141
23andMe allrs137853141
SNP Nexus

SNPshotrs137853141
SNPdbers137853141
MSV3drs137853141
GWAS Ctlgrs137853141
Max Magnitude0
OMIM604217
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853141(T;T)
Alt rs137853141(T;T)
Reference rs137853141(C;C)
Significance Pathogenic
Disease PULMONARY ALVEOLAR MICROLITHIASIS
Variation info
Gene SLC34A2
CLNDBN PULMONARY ALVEOLAR MICROLITHIASIS
Reversed 0
HGVS NC_000004.11:g.25664440C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006070.2,