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rs797044566

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044566(C;T)
Make rs797044566(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position6939141
GeneATN1
is asnp
is mentioned by
dbSNPrs797044566
ebirs797044566
HLIrs797044566
Exacrs797044566
Varsomers797044566
Maprs797044566
PheGenIrs797044566
hapmaprs797044566
1000 genomesrs797044566
hgdprs797044566
ensemblrs797044566
gopubmedrs797044566
geneviewrs797044566
scholarrs797044566
googlers797044566
pharmgkbrs797044566
gwascentralrs797044566
openSNPrs797044566
23andMers797044566
23andMe allrs797044566
SNP Nexus

SNPshotrs797044566
SNPdbers797044566
MSV3drs797044566
GWAS Ctlgrs797044566
Max Magnitude0
ClinVar
Risk rs797044566(T;T)
Alt rs797044566(T;T)
Reference rs797044566(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATN1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.7048304C>T
CLNSRC
CLNACC RCV000171467.1,