Have questions? Visit https://www.reddit.com/r/SNPedia

rs773730492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773730492(C;T)
Make rs773730492(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position84840372
GeneALPK3
is asnp
is mentioned by
dbSNPrs773730492
dbSNP (classic)rs773730492
ClinGenrs773730492
ebirs773730492
HLIrs773730492
Exacrs773730492
Gnomadrs773730492
Varsomers773730492
LitVarrs773730492
Maprs773730492
PheGenIrs773730492
Biobankrs773730492
1000 genomesrs773730492
hgdprs773730492
ensemblrs773730492
geneviewrs773730492
scholarrs773730492
googlers773730492
pharmgkbrs773730492
gwascentralrs773730492
openSNPrs773730492
23andMers773730492
SNPshotrs773730492
SNPdbers773730492
MSV3drs773730492
GWAS Ctlgrs773730492
Max Magnitude0
ClinVar
Risk rs773730492(T;T)
Alt rs773730492(T;T)
Reference Rs773730492(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALPK3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.85383603C>T
CLNSRC
CLNACC RCV000478156.1,