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rs1064796398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome21
Position32306744
GeneLOC105372779, MRAP
is asnp
is mentioned by
dbSNPrs1064796398
dbSNP (classic)rs1064796398
ClinGenrs1064796398
ebirs1064796398
HLIrs1064796398
Exacrs1064796398
Gnomadrs1064796398
Varsomers1064796398
LitVarrs1064796398
Maprs1064796398
PheGenIrs1064796398
Biobankrs1064796398
1000 genomesrs1064796398
hgdprs1064796398
ensemblrs1064796398
geneviewrs1064796398
scholarrs1064796398
googlers1064796398
pharmgkbrs1064796398
gwascentralrs1064796398
openSNPrs1064796398
23andMers1064796398
23andMe allrs1064796398
SNPshotrs1064796398
SNPdbers1064796398
MSV3drs1064796398
GWAS Ctlgrs1064796398
Max Magnitude0
ClinVar
Risk rs1064796398(T;T)
Alt rs1064796398(T;T)
Reference Rs1064796398(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MRAP
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.33679055G>T
CLNSRC
CLNACC RCV000482985.1,