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rs766090540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766090540(A;A)
Make rs766090540(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position43430098
GeneSZT2
is asnp
is mentioned by
dbSNPrs766090540
dbSNP (classic)rs766090540
ClinGenrs766090540
ebirs766090540
HLIrs766090540
Exacrs766090540
Gnomadrs766090540
Varsomers766090540
LitVarrs766090540
Maprs766090540
PheGenIrs766090540
Biobankrs766090540
1000 genomesrs766090540
hgdprs766090540
ensemblrs766090540
geneviewrs766090540
scholarrs766090540
googlers766090540
pharmgkbrs766090540
gwascentralrs766090540
openSNPrs766090540
23andMers766090540
SNPshotrs766090540
SNPdbers766090540
MSV3drs766090540
GWAS Ctlgrs766090540
Max Magnitude0
ClinVar
Risk rs766090540(A;A) rs766090540(T;T)
Alt rs766090540(A;A) rs766090540(T;T)
Reference Rs766090540(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SZT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43895769C>T
CLNSRC
CLNACC RCV000363038.1,