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rs755299132

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs755299132(C;T)
Make rs755299132(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position91220906
GeneAUH
is asnp
is mentioned by
dbSNPrs755299132
ebirs755299132
HLIrs755299132
Exacrs755299132
Varsomers755299132
Maprs755299132
PheGenIrs755299132
hapmaprs755299132
1000 genomesrs755299132
hgdprs755299132
ensemblrs755299132
gopubmedrs755299132
geneviewrs755299132
scholarrs755299132
googlers755299132
pharmgkbrs755299132
gwascentralrs755299132
openSNPrs755299132
23andMers755299132
23andMe allrs755299132
SNP Nexus

SNPshotrs755299132
SNPdbers755299132
MSV3drs755299132
GWAS Ctlgrs755299132
Max Magnitude0
ClinVar
Risk rs755299132(T;T)
Alt rs755299132(T;T)
Reference rs755299132(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AUH
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.93983188C>T
CLNSRC
CLNACC RCV000197560.1,