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rs796051990

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051990(A;G)
Make rs796051990(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71110040
GeneMCEE
is asnp
is mentioned by
dbSNPrs796051990
ebirs796051990
HLIrs796051990
Exacrs796051990
Varsomers796051990
Maprs796051990
PheGenIrs796051990
hapmaprs796051990
1000 genomesrs796051990
hgdprs796051990
ensemblrs796051990
gopubmedrs796051990
geneviewrs796051990
scholarrs796051990
googlers796051990
pharmgkbrs796051990
gwascentralrs796051990
openSNPrs796051990
23andMers796051990
23andMe allrs796051990
SNP Nexus

SNPshotrs796051990
SNPdbers796051990
MSV3drs796051990
GWAS Ctlgrs796051990
Max Magnitude0
ClinVar
Risk rs796051990(G;G)
Alt rs796051990(G;G)
Reference rs796051990(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MCEE
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.71337170T>C
CLNSRC
CLNACC RCV000186008.1,