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rs766466297

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs766466297(A;G)
Make rs766466297(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position57498563
GeneMARS
is asnp
is mentioned by
dbSNPrs766466297
ebirs766466297
HLIrs766466297
Exacrs766466297
Varsomers766466297
Maprs766466297
PheGenIrs766466297
hapmaprs766466297
1000 genomesrs766466297
hgdprs766466297
ensemblrs766466297
gopubmedrs766466297
geneviewrs766466297
scholarrs766466297
googlers766466297
pharmgkbrs766466297
gwascentralrs766466297
openSNPrs766466297
23andMers766466297
23andMe allrs766466297
SNP Nexus

SNPshotrs766466297
SNPdbers766466297
MSV3drs766466297
GWAS Ctlgrs766466297
Max Magnitude0
ClinVar
Risk rs766466297(G;G)
Alt rs766466297(G;G)
Reference rs766466297(A;A)
Significance Pathogenic
Disease Pulmonary alveolar proteinosis Interstitial lung and liver disease
Variation info
Gene MARS
CLNDBN Pulmonary alveolar proteinosis Interstitial lung and liver disease
Reversed 0
HGVS NC_000012.11:g.57892346A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000169767.1, RCV000172999.2,