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rs786205633

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205633(-;-)
Make rs786205633(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73448197
GeneALMS1
is asnp
is mentioned by
dbSNPrs786205633
ebirs786205633
HLIrs786205633
Exacrs786205633
Varsomers786205633
Maprs786205633
PheGenIrs786205633
hapmaprs786205633
1000 genomesrs786205633
hgdprs786205633
ensemblrs786205633
gopubmedrs786205633
geneviewrs786205633
scholarrs786205633
googlers786205633
pharmgkbrs786205633
gwascentralrs786205633
openSNPrs786205633
23andMers786205633
23andMe allrs786205633
SNP Nexus

SNPshotrs786205633
SNPdbers786205633
MSV3drs786205633
GWAS Ctlgrs786205633
Max Magnitude0
ClinVar
Risk rs786205633(;)
Alt rs786205633(;)
Reference rs786205633(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALMS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73675324delT
CLNSRC
CLNACC RCV000171495.1,