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rs757139660

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757139660(A;A)
Make rs757139660(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position73534828
GeneALMS1
is asnp
is mentioned by
dbSNPrs757139660
ebirs757139660
HLIrs757139660
Exacrs757139660
Varsomers757139660
Maprs757139660
PheGenIrs757139660
hapmaprs757139660
1000 genomesrs757139660
hgdprs757139660
ensemblrs757139660
gopubmedrs757139660
geneviewrs757139660
scholarrs757139660
googlers757139660
pharmgkbrs757139660
gwascentralrs757139660
openSNPrs757139660
23andMers757139660
23andMe allrs757139660
SNP Nexus

SNPshotrs757139660
SNPdbers757139660
MSV3drs757139660
GWAS Ctlgrs757139660
Max Magnitude0
ClinVar
Risk rs757139660(A;A)
Alt rs757139660(A;A)
Reference rs757139660(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALMS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73761955G>A
CLNSRC
CLNACC RCV000171295.1,