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rs1057519133

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519133(-;C)
Make rs1057519133(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position73490373
GeneALMS1
is asnp
is mentioned by
dbSNPrs1057519133
dbSNP (old)rs1057519133
ClinGenrs1057519133
ebirs1057519133
HLIrs1057519133
Exacrs1057519133
Gnomadrs1057519133
Varsomers1057519133
Maprs1057519133
PheGenIrs1057519133
Biobankrs1057519133
1000 genomesrs1057519133
hgdprs1057519133
ensemblrs1057519133
gopubmedrs1057519133
geneviewrs1057519133
scholarrs1057519133
googlers1057519133
pharmgkbrs1057519133
gwascentralrs1057519133
openSNPrs1057519133
23andMers1057519133
23andMe allrs1057519133
SNPshotrs1057519133
SNPdbers1057519133
MSV3drs1057519133
GWAS Ctlgrs1057519133
Max Magnitude0
ClinVar
Risk rs1057519133(C;C)
Alt rs1057519133(C;C)
Reference Rs1057519133(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALMS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73717500dupC
CLNSRC
CLNACC RCV000416189.1,