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rs1064795771

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position90561646
GeneMAP3K7
is asnp
is mentioned by
dbSNPrs1064795771
dbSNP (classic)rs1064795771
ClinGenrs1064795771
ebirs1064795771
HLIrs1064795771
Exacrs1064795771
Gnomadrs1064795771
Varsomers1064795771
LitVarrs1064795771
Maprs1064795771
PheGenIrs1064795771
Biobankrs1064795771
1000 genomesrs1064795771
hgdprs1064795771
ensemblrs1064795771
geneviewrs1064795771
scholarrs1064795771
googlers1064795771
pharmgkbrs1064795771
gwascentralrs1064795771
openSNPrs1064795771
23andMers1064795771
23andMe allrs1064795771
SNPshotrs1064795771
SNPdbers1064795771
MSV3drs1064795771
GWAS Ctlgrs1064795771
Max Magnitude0
ClinVar
Risk rs1064795771(A;A)
Alt rs1064795771(A;A)
Reference Rs1064795771(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP3K7
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.91271365C>T
CLNSRC
CLNACC RCV000478415.1,