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rs75399846

From SNPedia

Orientationplus
Stabilizedplus
Make rs75399846(C;C)
Make rs75399846(C;T)
Make rs75399846(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome10
Position100806519
GenePAX2
is asnp
is mentioned by
dbSNPrs75399846
dbSNP (classic)rs75399846
ClinGenrs75399846
ebirs75399846
HLIrs75399846
Exacrs75399846
Gnomadrs75399846
Varsomers75399846
LitVarrs75399846
Maprs75399846
PheGenIrs75399846
Biobankrs75399846
1000 genomesrs75399846
hgdprs75399846
ensemblrs75399846
geneviewrs75399846
scholarrs75399846
googlers75399846
pharmgkbrs75399846
gwascentralrs75399846
openSNPrs75399846
23andMers75399846
23andMe allrs75399846
SNPshotrs75399846
SNPdbers75399846
MSV3drs75399846
GWAS Ctlgrs75399846
Max Magnitude0

aka NM_000278.4(PAX2):c.706C>T or (p.Gln236Ter)

OMIM pathogenic variant