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rs121912988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912988(G;G)
Make rs121912988(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position87610924
GeneDSPP
is asnp
is mentioned by
dbSNPrs121912988
ebirs121912988
HLIrs121912988
Exacrs121912988
Varsomers121912988
Maprs121912988
PheGenIrs121912988
hapmaprs121912988
1000 genomesrs121912988
hgdprs121912988
ensemblrs121912988
gopubmedrs121912988
geneviewrs121912988
scholarrs121912988
googlers121912988
pharmgkbrs121912988
gwascentralrs121912988
openSNPrs121912988
23andMers121912988
23andMe allrs121912988
SNP Nexus

SNPshotrs121912988
SNPdbers121912988
MSV3drs121912988
GWAS Ctlgrs121912988
Max Magnitude0
OMIM125485
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121912988(G;G)
Alt rs121912988(G;G)
Reference rs121912988(T;T)
Significance Pathogenic
Disease Denticles
Variation info
Gene DSPP
CLNDBN Denticles
Reversed 0
HGVS NC_000004.11:g.88532076T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018353.27,