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rs773073663

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773073663(C;T)
Make rs773073663(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127819899
GeneENG
is asnp
is mentioned by
dbSNPrs773073663
ebirs773073663
HLIrs773073663
Exacrs773073663
Varsomers773073663
Maprs773073663
PheGenIrs773073663
hapmaprs773073663
1000 genomesrs773073663
hgdprs773073663
ensemblrs773073663
gopubmedrs773073663
geneviewrs773073663
scholarrs773073663
googlers773073663
pharmgkbrs773073663
gwascentralrs773073663
openSNPrs773073663
23andMers773073663
23andMe allrs773073663
SNP Nexus

SNPshotrs773073663
SNPdbers773073663
MSV3drs773073663
GWAS Ctlgrs773073663
Max Magnitude0
ClinVar
Risk rs773073663(A,T;A,T)
Alt rs773073663(A,T;A,T)
Reference rs773073663(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130582178C>T
CLNSRC
CLNACC RCV000196088.1,