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rs869312733

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312733(A;C)
Make rs869312733(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position32940899
GeneTMEM98
is asnp
is mentioned by
dbSNPrs869312733
ebirs869312733
HLIrs869312733
Exacrs869312733
Varsomers869312733
Maprs869312733
PheGenIrs869312733
hapmaprs869312733
1000 genomesrs869312733
hgdprs869312733
ensemblrs869312733
gopubmedrs869312733
geneviewrs869312733
scholarrs869312733
googlers869312733
pharmgkbrs869312733
gwascentralrs869312733
openSNPrs869312733
23andMers869312733
23andMe allrs869312733
SNP Nexus

SNPshotrs869312733
SNPdbers869312733
MSV3drs869312733
GWAS Ctlgrs869312733
Max Magnitude0
ClinVar
Risk rs869312733(C;C)
Alt rs869312733(C;C)
Reference rs869312733(A;A)
Significance Pathogenic
Disease Nanophthalmos 4
Variation info
Gene TMEM98
CLNDBN Nanophthalmos 4
Reversed 0
HGVS NC_000017.10:g.31267917A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210025.2,