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rs797045228

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045228(-;A)
Make rs797045228(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73450680
GeneALMS1
is asnp
is mentioned by
dbSNPrs797045228
dbSNP (old)rs797045228
ClinGenrs797045228
ebirs797045228
HLIrs797045228
Exacrs797045228
Varsomers797045228
Maprs797045228
PheGenIrs797045228
Biobankrs797045228
1000 genomesrs797045228
hgdprs797045228
ensemblrs797045228
gopubmedrs797045228
geneviewrs797045228
scholarrs797045228
googlers797045228
pharmgkbrs797045228
gwascentralrs797045228
openSNPrs797045228
23andMers797045228
23andMe allrs797045228
SNP Nexus

SNPshotrs797045228
SNPdbers797045228
MSV3drs797045228
GWAS Ctlgrs797045228
Max Magnitude0
ClinVar
Risk rs797045228(A;A)
Alt rs797045228(A;A)
Reference Rs797045228(-;-)
Significance Pathogenic
Disease Alstrom syndrome
Variation info
Gene ALMS1
CLNDBN Alstrom syndrome
Reversed 0
HGVS NC_000002.11:g.73677807dupA
CLNSRC
CLNACC RCV000194605.1,