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rs863223956

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs863223956(-;-)
Make rs863223956(-;CA)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position43508053
GeneETHE1
is asnp
is mentioned by
dbSNPrs863223956
dbSNP (classic)rs863223956
ClinGenrs863223956
ebirs863223956
HLIrs863223956
Exacrs863223956
Gnomadrs863223956
Varsomers863223956
LitVarrs863223956
Maprs863223956
PheGenIrs863223956
Biobankrs863223956
1000 genomesrs863223956
hgdprs863223956
ensemblrs863223956
geneviewrs863223956
scholarrs863223956
googlers863223956
pharmgkbrs863223956
gwascentralrs863223956
openSNPrs863223956
23andMers863223956
SNPshotrs863223956
SNPdbers863223956
MSV3drs863223956
GWAS Ctlgrs863223956
Max Magnitude0
ClinVar
Risk rs863223956(-;-)
Alt rs863223956(-;-)
Reference Rs863223956(CA;CA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETHE1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.44012205_44012206delTG
CLNSRC
CLNACC RCV000197919.1,