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rs786205527

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205527(A;T)
Make rs786205527(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position73601193
GeneALMS1
is asnp
is mentioned by
dbSNPrs786205527
ebirs786205527
HLIrs786205527
Exacrs786205527
Varsomers786205527
Maprs786205527
PheGenIrs786205527
hapmaprs786205527
1000 genomesrs786205527
hgdprs786205527
ensemblrs786205527
gopubmedrs786205527
geneviewrs786205527
scholarrs786205527
googlers786205527
pharmgkbrs786205527
gwascentralrs786205527
openSNPrs786205527
23andMers786205527
23andMe allrs786205527
SNP Nexus

SNPshotrs786205527
SNPdbers786205527
MSV3drs786205527
GWAS Ctlgrs786205527
Max Magnitude0
ClinVar
Risk rs786205527(T;T)
Alt rs786205527(T;T)
Reference rs786205527(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALMS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73828320A>T
CLNSRC
CLNACC RCV000171296.1,