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rs756021768

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs756021768(A;G)
Make rs756021768(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position57512811
GeneMARS, MIR6758
is asnp
is mentioned by
dbSNPrs756021768
ebirs756021768
HLIrs756021768
Exacrs756021768
Varsomers756021768
Maprs756021768
PheGenIrs756021768
hapmaprs756021768
1000 genomesrs756021768
hgdprs756021768
ensemblrs756021768
gopubmedrs756021768
geneviewrs756021768
scholarrs756021768
googlers756021768
pharmgkbrs756021768
gwascentralrs756021768
openSNPrs756021768
23andMers756021768
23andMe allrs756021768
SNP Nexus

SNPshotrs756021768
SNPdbers756021768
MSV3drs756021768
GWAS Ctlgrs756021768
Max Magnitude0
ClinVar
Risk rs756021768(G,T;G,T)
Alt rs756021768(G,T;G,T)
Reference rs756021768(A;A)
Significance Pathogenic
Disease Pulmonary alveolar proteinosis Interstitial lung and liver disease
Variation info
Gene MARS MIR6758
CLNDBN Pulmonary alveolar proteinosis Interstitial lung and liver disease
Reversed 0
HGVS NC_000012.11:g.57906594A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000169766.1, RCV000173001.2,