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rs13076312

From SNPedia

Orientationplus
Stabilizedplus
Make rs13076312(C;C)
Make rs13076312(C;T)
Make rs13076312(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position188371466
GeneLPP
is asnp
is mentioned by
dbSNPrs13076312
dbSNP (classic)rs13076312
ClinGenrs13076312
ebirs13076312
HLIrs13076312
Exacrs13076312
Gnomadrs13076312
Varsomers13076312
LitVarrs13076312
Maprs13076312
PheGenIrs13076312
Biobankrs13076312
1000 genomesrs13076312
hgdprs13076312
ensemblrs13076312
geneviewrs13076312
scholarrs13076312
googlers13076312
pharmgkbrs13076312
gwascentralrs13076312
openSNPrs13076312
23andMers13076312
23andMe allrs13076312
SNPshotrs13076312
SNPdbers13076312
MSV3drs13076312
GWAS Ctlgrs13076312
GMAF0.4945
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Generalized Vitiligo


[PMID 18311140OA-icon.png] Newly identified genetic risk variants for celiac disease related to the immune response.