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rs863223954

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223954(A;G)
Make rs863223954(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position43508062
GeneETHE1
is asnp
is mentioned by
dbSNPrs863223954
ebirs863223954
HLIrs863223954
Exacrs863223954
Varsomers863223954
Maprs863223954
PheGenIrs863223954
hapmaprs863223954
1000 genomesrs863223954
hgdprs863223954
ensemblrs863223954
gopubmedrs863223954
geneviewrs863223954
scholarrs863223954
googlers863223954
pharmgkbrs863223954
gwascentralrs863223954
openSNPrs863223954
23andMers863223954
23andMe allrs863223954
SNP Nexus

SNPshotrs863223954
SNPdbers863223954
MSV3drs863223954
GWAS Ctlgrs863223954
Max Magnitude0
ClinVar
Risk rs863223954(G;G)
Alt rs863223954(G;G)
Reference rs863223954(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ETHE1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.44012214T>C
CLNSRC
CLNACC RCV000196876.1,