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rs786205619

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205619(-;-)
Make rs786205619(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position64759194
GeneGNS
is asnp
is mentioned by
dbSNPrs786205619
ebirs786205619
HLIrs786205619
Exacrs786205619
Varsomers786205619
Maprs786205619
PheGenIrs786205619
hapmaprs786205619
1000 genomesrs786205619
hgdprs786205619
ensemblrs786205619
gopubmedrs786205619
geneviewrs786205619
scholarrs786205619
googlers786205619
pharmgkbrs786205619
gwascentralrs786205619
openSNPrs786205619
23andMers786205619
23andMe allrs786205619
SNP Nexus

SNPshotrs786205619
SNPdbers786205619
MSV3drs786205619
GWAS Ctlgrs786205619
Max Magnitude0
ClinVar
Risk rs786205619(;)
Alt rs786205619(;)
Reference rs786205619(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNS
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.65152974delA
CLNSRC
CLNACC RCV000171468.1,