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rs1064793754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGT;AAGT) 0 common in clinvar
Chromosome1
Position108922579
GeneGPSM2
is asnp
is mentioned by
dbSNPrs1064793754
dbSNP (classic)rs1064793754
ClinGenrs1064793754
ebirs1064793754
HLIrs1064793754
Exacrs1064793754
Gnomadrs1064793754
Varsomers1064793754
LitVarrs1064793754
Maprs1064793754
PheGenIrs1064793754
Biobankrs1064793754
1000 genomesrs1064793754
hgdprs1064793754
ensemblrs1064793754
geneviewrs1064793754
scholarrs1064793754
googlers1064793754
pharmgkbrs1064793754
gwascentralrs1064793754
openSNPrs1064793754
23andMers1064793754
SNPshotrs1064793754
SNPdbers1064793754
MSV3drs1064793754
GWAS Ctlgrs1064793754
Max Magnitude0
ClinVar
Risk rs1064793754(-;-)
Alt rs1064793754(-;-)
Reference Rs1064793754(AAGT;AAGT)
Significance Pathogenic
Disease not provided
Variation info
Gene GPSM2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.109465201_109465204delAAGT
CLNSRC
CLNACC RCV000487382.1,