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rs177216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs177216(A;A)
Make rs177216(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position78063343
is asnp
is mentioned by
dbSNPrs177216
ebirs177216
HLIrs177216
Exacrs177216
Varsomers177216
Maprs177216
PheGenIrs177216
hapmaprs177216
1000 genomesrs177216
hgdprs177216
ensemblrs177216
gopubmedrs177216
geneviewrs177216
scholarrs177216
googlers177216
pharmgkbrs177216
gwascentralrs177216
openSNPrs177216
23andMers177216
23andMe allrs177216
SNP Nexus

SNPshotrs177216
SNPdbers177216
MSV3drs177216
GWAS Ctlgrs177216
GMAF0.1056
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 21622161] Confirmation and further mapping of the GLC3C locus in primary congenital glaucoma.