Have questions? Visit https://www.reddit.com/r/SNPedia

rs104893862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893862(A;A)
Make rs104893862(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position110621231
GenePITX2
is asnp
is mentioned by
dbSNPrs104893862
ebirs104893862
HLIrs104893862
Exacrs104893862
Varsomers104893862
Maprs104893862
PheGenIrs104893862
hapmaprs104893862
1000 genomesrs104893862
hgdprs104893862
ensemblrs104893862
gopubmedrs104893862
geneviewrs104893862
scholarrs104893862
googlers104893862
pharmgkbrs104893862
gwascentralrs104893862
openSNPrs104893862
23andMers104893862
23andMe allrs104893862
SNP Nexus

SNPshotrs104893862
SNPdbers104893862
MSV3drs104893862
GWAS Ctlgrs104893862
Max Magnitude0
OMIM601542
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104893862(A;A)
Alt rs104893862(A;A)
Reference rs104893862(G;G)
Significance Pathogenic
Disease Ring dermoid of cornea
Variation info
Gene PITX2
CLNDBN Ring dermoid of cornea
Reversed 1
HGVS NC_000004.11:g.111542387C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008562.2,