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rs118203958

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203958(C;T)
Make rs118203958(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position74190889
GeneSTRA6
is asnp
is mentioned by
dbSNPrs118203958
ebirs118203958
HLIrs118203958
Exacrs118203958
Varsomers118203958
Maprs118203958
PheGenIrs118203958
hapmaprs118203958
1000 genomesrs118203958
hgdprs118203958
ensemblrs118203958
gopubmedrs118203958
geneviewrs118203958
scholarrs118203958
googlers118203958
pharmgkbrs118203958
gwascentralrs118203958
openSNPrs118203958
23andMers118203958
23andMe allrs118203958
SNP Nexus

SNPshotrs118203958
SNPdbers118203958
MSV3drs118203958
GWAS Ctlgrs118203958
Max Magnitude0
OMIM610745
Desc
Variant0001
Relatedalso
ClinVar
Risk rs118203958(T;T)
Alt rs118203958(T;T)
Reference rs118203958(C;C)
Significance Pathogenic
Disease Microphthalmia syndromic 9
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9
Reversed 1
HGVS NC_000015.9:g.74483230G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001192.2,