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rs1057517758

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517758(A;A)
Make rs1057517758(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position90556586
GeneMAP3K7
is asnp
is mentioned by
dbSNPrs1057517758
dbSNP (old)rs1057517758
ClinGenrs1057517758
ebirs1057517758
HLIrs1057517758
Exacrs1057517758
Gnomadrs1057517758
Varsomers1057517758
Maprs1057517758
PheGenIrs1057517758
Biobankrs1057517758
1000 genomesrs1057517758
hgdprs1057517758
ensemblrs1057517758
gopubmedrs1057517758
geneviewrs1057517758
scholarrs1057517758
googlers1057517758
pharmgkbrs1057517758
gwascentralrs1057517758
openSNPrs1057517758
23andMers1057517758
23andMe allrs1057517758
SNPshotrs1057517758
SNPdbers1057517758
MSV3drs1057517758
GWAS Ctlgrs1057517758
Max Magnitude0
ClinVar
Risk rs1057517758(A;A)
Alt rs1057517758(A;A)
Reference Rs1057517758(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP3K7
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.91266305C>T
CLNSRC
CLNACC RCV000414538.1,