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rs10129516

From SNPedia

Orientationplus
Stabilizedplus
Make rs10129516(C;C)
Make rs10129516(C;T)
Make rs10129516(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position63133372
GeneLOC105370531
is asnp
is mentioned by
dbSNPrs10129516
dbSNP (old)rs10129516
ClinGenrs10129516
ebirs10129516
HLIrs10129516
Exacrs10129516
Gnomadrs10129516
Varsomers10129516
LitVarrs10129516
Maprs10129516
PheGenIrs10129516
Biobankrs10129516
1000 genomesrs10129516
hgdprs10129516
ensemblrs10129516
gopubmedrs10129516
geneviewrs10129516
scholarrs10129516
googlers10129516
pharmgkbrs10129516
gwascentralrs10129516
openSNPrs10129516
23andMers10129516
23andMe allrs10129516
SNPshotrs10129516
SNPdbers10129516
MSV3drs10129516
GWAS Ctlgrs10129516
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 28881265] New variants near RHOJ and C2, HLA-DRA region and susceptibility to endometriosis in the Polish population-The genome-wide association study.