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rs7052177

From SNPedia

Orientationplus
Stabilizedplus
Make rs7052177(G;G)
Make rs7052177(G;T)
Make rs7052177(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position23356765
GenePTCHD1
is asnp
is mentioned by
dbSNPrs7052177
ebirs7052177
HLIrs7052177
Exacrs7052177
Varsomers7052177
Maprs7052177
PheGenIrs7052177
hapmaprs7052177
1000 genomesrs7052177
hgdprs7052177
ensemblrs7052177
gopubmedrs7052177
geneviewrs7052177
scholarrs7052177
googlers7052177
pharmgkbrs7052177
gwascentralrs7052177
openSNPrs7052177
23andMers7052177
23andMe allrs7052177
SNP Nexus

SNPshotrs7052177
SNPdbers7052177
MSV3drs7052177
GWAS Ctlgrs7052177
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 25782667] Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability