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rs768669208

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768669208(C;T)
Make rs768669208(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position43511466
GeneETHE1
is asnp
is mentioned by
dbSNPrs768669208
ebirs768669208
HLIrs768669208
Exacrs768669208
Varsomers768669208
Maprs768669208
PheGenIrs768669208
hapmaprs768669208
1000 genomesrs768669208
hgdprs768669208
ensemblrs768669208
gopubmedrs768669208
geneviewrs768669208
scholarrs768669208
googlers768669208
pharmgkbrs768669208
gwascentralrs768669208
openSNPrs768669208
23andMers768669208
23andMe allrs768669208
SNP Nexus

SNPshotrs768669208
SNPdbers768669208
MSV3drs768669208
GWAS Ctlgrs768669208
Max Magnitude0
ClinVar
Risk rs768669208(T;T)
Alt rs768669208(T;T)
Reference rs768669208(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETHE1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.44015618C>T
CLNSRC
CLNACC RCV000199428.1,