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rs967293

From SNPedia

Orientationplus
Stabilizedplus
Make rs967293(C;C)
Make rs967293(C;G)
Make rs967293(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position33831897
GeneASIC2
is asnp
is mentioned by
dbSNPrs967293
ebirs967293
HLIrs967293
Exacrs967293
Varsomers967293
Maprs967293
PheGenIrs967293
hapmaprs967293
1000 genomesrs967293
hgdprs967293
ensemblrs967293
gopubmedrs967293
geneviewrs967293
scholarrs967293
googlers967293
pharmgkbrs967293
gwascentralrs967293
openSNPrs967293
23andMers967293
23andMe allrs967293
SNP Nexus

SNPshotrs967293
SNPdbers967293
MSV3drs967293
GWAS Ctlgrs967293
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 24852644] Mutation in TMEM98 in a Large White Kindred With Autosomal Dominant Nanophthalmos Linked to 17p12-q12