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rs765256758

From SNPedia

Orientationplus
Stabilizedplus
Make rs765256758(C;C)
Make rs765256758(C;T)
Make rs765256758(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome3
Position190402428
GeneCLDN16
is asnp
is mentioned by
dbSNPrs765256758
dbSNP (classic)rs765256758
ClinGenrs765256758
ebirs765256758
HLIrs765256758
Exacrs765256758
Gnomadrs765256758
Varsomers765256758
LitVarrs765256758
Maprs765256758
PheGenIrs765256758
Biobankrs765256758
1000 genomesrs765256758
hgdprs765256758
ensemblrs765256758
geneviewrs765256758
scholarrs765256758
googlers765256758
pharmgkbrs765256758
gwascentralrs765256758
openSNPrs765256758
23andMers765256758
23andMe allrs765256758
SNPshotrs765256758
SNPdbers765256758
MSV3drs765256758
GWAS Ctlgrs765256758
Max Magnitude0

aka NM_006580.3(CLDN16):c.416C>T or (p.Ala139Val)

OMIM pathogenic variant