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rs121434308

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434308(A;A)
Make rs121434308(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position48411988
GeneLPAR6, RB1
is asnp
is mentioned by
dbSNPrs121434308
ebirs121434308
HLIrs121434308
Exacrs121434308
Varsomers121434308
Maprs121434308
PheGenIrs121434308
hapmaprs121434308
1000 genomesrs121434308
hgdprs121434308
ensemblrs121434308
gopubmedrs121434308
geneviewrs121434308
scholarrs121434308
googlers121434308
pharmgkbrs121434308
gwascentralrs121434308
openSNPrs121434308
23andMers121434308
23andMe allrs121434308
SNP Nexus

SNPshotrs121434308
SNPdbers121434308
MSV3drs121434308
GWAS Ctlgrs121434308
Max Magnitude0
OMIM609239
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121434308(A;A)
Alt rs121434308(A;A)
Reference rs121434308(G;G)
Significance Pathogenic
Disease Hypotrichosis 8
Variation info
Gene RB1 LPAR6
CLNDBN Hypotrichosis 8
Reversed 1
HGVS NC_000013.10:g.48986124C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001902.2,