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rs137853142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853142(C;C)
Make rs137853142(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position25664267
GeneSLC34A2
is asnp
is mentioned by
dbSNPrs137853142
ebirs137853142
HLIrs137853142
Exacrs137853142
Varsomers137853142
Maprs137853142
PheGenIrs137853142
hapmaprs137853142
1000 genomesrs137853142
hgdprs137853142
ensemblrs137853142
gopubmedrs137853142
geneviewrs137853142
scholarrs137853142
googlers137853142
pharmgkbrs137853142
gwascentralrs137853142
openSNPrs137853142
23andMers137853142
23andMe allrs137853142
SNP Nexus

SNPshotrs137853142
SNPdbers137853142
MSV3drs137853142
GWAS Ctlgrs137853142
Max Magnitude0
OMIM604217
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853142(A,C;A,C)
Alt rs137853142(A,C;A,C)
Reference rs137853142(G;G)
Significance Pathogenic
Disease PULMONARY ALVEOLAR MICROLITHIASIS
Variation info
Gene SLC34A2
CLNDBN PULMONARY ALVEOLAR MICROLITHIASIS
Reversed 0
HGVS NC_000004.11:g.25665889G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006071.2,