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rs797044892

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044892(C;C)
Make rs797044892(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position21805938
GeneMAPK1
is asnp
is mentioned by
dbSNPrs797044892
ebirs797044892
HLIrs797044892
Exacrs797044892
Varsomers797044892
Maprs797044892
PheGenIrs797044892
hapmaprs797044892
1000 genomesrs797044892
hgdprs797044892
ensemblrs797044892
gopubmedrs797044892
geneviewrs797044892
scholarrs797044892
googlers797044892
pharmgkbrs797044892
gwascentralrs797044892
openSNPrs797044892
23andMers797044892
23andMe allrs797044892
SNP Nexus

SNPshotrs797044892
SNPdbers797044892
MSV3drs797044892
GWAS Ctlgrs797044892
Max Magnitude0
ClinVar
Risk rs797044892(C;C)
Alt rs797044892(C;C)
Reference rs797044892(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene MAPK1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000022.10:g.22160227C>G
CLNSRC
CLNACC RCV000190714.1,