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rs118203953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203953(C;G)
Make rs118203953(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11285822
GeneUBIAD1
is asnp
is mentioned by
dbSNPrs118203953
ebirs118203953
HLIrs118203953
Exacrs118203953
Varsomers118203953
Maprs118203953
PheGenIrs118203953
hapmaprs118203953
1000 genomesrs118203953
hgdprs118203953
ensemblrs118203953
gopubmedrs118203953
geneviewrs118203953
scholarrs118203953
googlers118203953
pharmgkbrs118203953
gwascentralrs118203953
openSNPrs118203953
23andMers118203953
23andMe allrs118203953
SNP Nexus

SNPshotrs118203953
SNPdbers118203953
MSV3drs118203953
GWAS Ctlgrs118203953
Max Magnitude0
OMIM611632
Desc
Variant0009
Relatedalso
ClinVar
Risk rs118203953(G;G)
Alt rs118203953(G;G)
Reference rs118203953(C;C)
Significance Pathogenic
Disease Schnyder crystalline corneal dystrophy
Variation info
Gene UBIAD1
CLNDBN Schnyder crystalline corneal dystrophy
Reversed 0
HGVS NC_000001.10:g.11345879C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000912.2,