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rs149956316

From SNPedia

Orientationplus
Stabilizedplus
Make rs149956316(A;A)
Make rs149956316(A;G)
Make rs149956316(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position110706284
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs149956316
dbSNP (old)rs149956316
ClinGenrs149956316
ebirs149956316
HLIrs149956316
Exacrs149956316
Varsomers149956316
Maprs149956316
PheGenIrs149956316
Biobankrs149956316
1000 genomesrs149956316
hgdprs149956316
ensemblrs149956316
gopubmedrs149956316
geneviewrs149956316
scholarrs149956316
googlers149956316
pharmgkbrs149956316
gwascentralrs149956316
openSNPrs149956316
23andMers149956316
23andMe allrs149956316
SNP Nexus

SNPshotrs149956316
SNPdbers149956316
MSV3drs149956316
GWAS Ctlgrs149956316
Max Magnitude

[PMID 25093588OA-icon.png] Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness