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rs770558150

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770558150(C;T)
Make rs770558150(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73452960
GeneALMS1
is asnp
is mentioned by
dbSNPrs770558150
ebirs770558150
HLIrs770558150
Exacrs770558150
Varsomers770558150
Maprs770558150
PheGenIrs770558150
hapmaprs770558150
1000 genomesrs770558150
hgdprs770558150
ensemblrs770558150
gopubmedrs770558150
geneviewrs770558150
scholarrs770558150
googlers770558150
pharmgkbrs770558150
gwascentralrs770558150
openSNPrs770558150
23andMers770558150
23andMe allrs770558150
SNP Nexus

SNPshotrs770558150
SNPdbers770558150
MSV3drs770558150
GWAS Ctlgrs770558150
Max Magnitude0
ClinVar
Risk rs770558150(T;T)
Alt rs770558150(T;T)
Reference rs770558150(C;C)
Significance Pathogenic
Disease Alstrom syndrome
Variation info
Gene ALMS1
CLNDBN Alstrom syndrome
Reversed 0
HGVS NC_000002.11:g.73680087C>T
CLNSRC
CLNACC RCV000194023.1,