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rs786205526

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205526(A;A)
Make rs786205526(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73422974
GeneALMS1
is asnp
is mentioned by
dbSNPrs786205526
ebirs786205526
HLIrs786205526
Exacrs786205526
Varsomers786205526
Maprs786205526
PheGenIrs786205526
hapmaprs786205526
1000 genomesrs786205526
hgdprs786205526
ensemblrs786205526
gopubmedrs786205526
geneviewrs786205526
scholarrs786205526
googlers786205526
pharmgkbrs786205526
gwascentralrs786205526
openSNPrs786205526
23andMers786205526
23andMe allrs786205526
SNP Nexus

SNPshotrs786205526
SNPdbers786205526
MSV3drs786205526
GWAS Ctlgrs786205526
Max Magnitude0
ClinVar
Risk rs786205526(A;A)
Alt rs786205526(A;A)
Reference rs786205526(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALMS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73650102G>A
CLNSRC
CLNACC RCV000171293.1,