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rs746640196

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746640196(C;T)
Make rs746640196(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position73449253
GeneALMS1
is asnp
is mentioned by
dbSNPrs746640196
ebirs746640196
HLIrs746640196
Exacrs746640196
Varsomers746640196
Maprs746640196
PheGenIrs746640196
hapmaprs746640196
1000 genomesrs746640196
hgdprs746640196
ensemblrs746640196
gopubmedrs746640196
geneviewrs746640196
scholarrs746640196
googlers746640196
pharmgkbrs746640196
gwascentralrs746640196
openSNPrs746640196
23andMers746640196
23andMe allrs746640196
SNP Nexus

SNPshotrs746640196
SNPdbers746640196
MSV3drs746640196
GWAS Ctlgrs746640196
Max Magnitude0
ClinVar
Risk rs746640196(T;T)
Alt rs746640196(T;T)
Reference rs746640196(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALMS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73676380C>G
CLNSRC
CLNACC RCV000171294.1,