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rs772136379

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs772136379(G;G)
Make rs772136379(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73451669
GeneALMS1
is asnp
is mentioned by
dbSNPrs772136379
ebirs772136379
HLIrs772136379
Exacrs772136379
Varsomers772136379
Maprs772136379
PheGenIrs772136379
hapmaprs772136379
1000 genomesrs772136379
hgdprs772136379
ensemblrs772136379
gopubmedrs772136379
geneviewrs772136379
scholarrs772136379
googlers772136379
pharmgkbrs772136379
gwascentralrs772136379
openSNPrs772136379
23andMers772136379
23andMe allrs772136379
SNP Nexus

SNPshotrs772136379
SNPdbers772136379
MSV3drs772136379
GWAS Ctlgrs772136379
Max Magnitude0
ClinVar
Risk rs772136379(G;G)
Alt rs772136379(G;G)
Reference rs772136379(T;T)
Significance Probable-Pathogenic
Disease Alstrom syndrome
Variation info
Gene ALMS1
CLNDBN Alstrom syndrome
Reversed 0
HGVS NC_000002.11:g.73678796T>G
CLNSRC
CLNACC RCV000192391.1,