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rs201912053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201912053(A;A)
Make rs201912053(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position32989768
GeneAPTX
is asnp
is mentioned by
dbSNPrs201912053
dbSNP (classic)rs201912053
ClinGenrs201912053
ebirs201912053
HLIrs201912053
Exacrs201912053
Gnomadrs201912053
Varsomers201912053
LitVarrs201912053
Maprs201912053
PheGenIrs201912053
Biobankrs201912053
1000 genomesrs201912053
hgdprs201912053
ensemblrs201912053
geneviewrs201912053
scholarrs201912053
googlers201912053
pharmgkbrs201912053
gwascentralrs201912053
openSNPrs201912053
23andMers201912053
23andMe allrs201912053
SNPshotrs201912053
SNPdbers201912053
MSV3drs201912053
GWAS Ctlgrs201912053
Max Magnitude0
ClinVar
Risk rs201912053(A;A)
Alt rs201912053(A;A)
Reference Rs201912053(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene APTX
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.32989766G>A
CLNSRC
CLNACC RCV000480449.1,