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rs121434306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434306(C;T)
Make rs121434306(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48411961
GeneLPAR6, RB1
is asnp
is mentioned by
dbSNPrs121434306
ebirs121434306
HLIrs121434306
Exacrs121434306
Varsomers121434306
Maprs121434306
PheGenIrs121434306
hapmaprs121434306
1000 genomesrs121434306
hgdprs121434306
ensemblrs121434306
gopubmedrs121434306
geneviewrs121434306
scholarrs121434306
googlers121434306
pharmgkbrs121434306
gwascentralrs121434306
openSNPrs121434306
23andMers121434306
23andMe allrs121434306
SNP Nexus

SNPshotrs121434306
SNPdbers121434306
MSV3drs121434306
GWAS Ctlgrs121434306
Max Magnitude0
OMIM609239
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434306(T;T)
Alt rs121434306(T;T)
Reference rs121434306(C;C)
Significance Pathogenic
Disease Hypotrichosis 8
Variation info
Gene RB1 LPAR6
CLNDBN Hypotrichosis 8
Reversed 1
HGVS NC_000013.10:g.48986097G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001898.2,