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rs587777690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777690(C;C)
Make rs587777690(C;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position32940889
GeneTMEM98
is asnp
is mentioned by
dbSNPrs587777690
ebirs587777690
HLIrs587777690
Exacrs587777690
Varsomers587777690
Maprs587777690
PheGenIrs587777690
hapmaprs587777690
1000 genomesrs587777690
hgdprs587777690
ensemblrs587777690
gopubmedrs587777690
geneviewrs587777690
scholarrs587777690
googlers587777690
pharmgkbrs587777690
gwascentralrs587777690
openSNPrs587777690
23andMers587777690
23andMe allrs587777690
SNP Nexus

SNPshotrs587777690
SNPdbers587777690
MSV3drs587777690
GWAS Ctlgrs587777690
Max Magnitude0
ClinVar
Risk rs587777690(C;C)
Alt rs587777690(C;C)
Reference rs587777690(G;G)
Significance Pathogenic
Disease Nanophthalmos 4
Variation info
Gene TMEM98
CLNDBN Nanophthalmos 4
Reversed 0
HGVS NC_000017.10:g.31267907G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000143786.3,