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rs878855003

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878855003(-;-)
Make rs878855003(-;A)
Make rs878855003(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position73491389
GeneALMS1
is asnp
is mentioned by
dbSNPrs878855003
ebirs878855003
HLIrs878855003
Exacrs878855003
Varsomers878855003
Maprs878855003
PheGenIrs878855003
hapmaprs878855003
1000 genomesrs878855003
hgdprs878855003
ensemblrs878855003
gopubmedrs878855003
geneviewrs878855003
scholarrs878855003
googlers878855003
pharmgkbrs878855003
gwascentralrs878855003
openSNPrs878855003
23andMers878855003
23andMe allrs878855003
SNP Nexus

SNPshotrs878855003
SNPdbers878855003
MSV3drs878855003
GWAS Ctlgrs878855003
Max Magnitude0
ClinVar
Risk rs878855003(A;A)
Alt rs878855003(A;A)
Reference rs878855003(;)
Significance Pathogenic
Disease Alstrom syndrome
Variation info
Gene ALMS1
CLNDBN Alstrom syndrome
Reversed 0
HGVS NC_000002.11:g.73718516dupA
CLNSRC
CLNACC RCV000233354.1,