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rs786205563

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205563(A;A)
Make rs786205563(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position94039955
GeneARL13B
is asnp
is mentioned by
dbSNPrs786205563
ebirs786205563
HLIrs786205563
Exacrs786205563
Varsomers786205563
Maprs786205563
PheGenIrs786205563
hapmaprs786205563
1000 genomesrs786205563
hgdprs786205563
ensemblrs786205563
gopubmedrs786205563
geneviewrs786205563
scholarrs786205563
googlers786205563
pharmgkbrs786205563
gwascentralrs786205563
openSNPrs786205563
23andMers786205563
23andMe allrs786205563
SNP Nexus

SNPshotrs786205563
SNPdbers786205563
MSV3drs786205563
GWAS Ctlgrs786205563
Max Magnitude0
ClinVar
Risk rs786205563(A;A)
Alt rs786205563(A;A)
Reference rs786205563(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARL13B
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.93758799T>A
CLNSRC
CLNACC RCV000171363.1,