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rs765909830

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765909830(A;A)
Make rs765909830(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position160128782
GeneATP1A2
is asnp
is mentioned by
dbSNPrs765909830
ebirs765909830
HLIrs765909830
Exacrs765909830
Varsomers765909830
Maprs765909830
PheGenIrs765909830
hapmaprs765909830
1000 genomesrs765909830
hgdprs765909830
ensemblrs765909830
gopubmedrs765909830
geneviewrs765909830
scholarrs765909830
googlers765909830
pharmgkbrs765909830
gwascentralrs765909830
openSNPrs765909830
23andMers765909830
23andMe allrs765909830
SNP Nexus

SNPshotrs765909830
SNPdbers765909830
MSV3drs765909830
GWAS Ctlgrs765909830
Max Magnitude0
ClinVar
Risk rs765909830(A;A)
Alt rs765909830(A;A)
Reference rs765909830(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP1A2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.160098572G>A
CLNSRC
CLNACC RCV000186788.1,