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rs879255262

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255262(A;T)
Make rs879255262(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position48412236
GeneLPAR6, RB1
is asnp
is mentioned by
dbSNPrs879255262
ebirs879255262
HLIrs879255262
Exacrs879255262
Varsomers879255262
Maprs879255262
PheGenIrs879255262
hapmaprs879255262
1000 genomesrs879255262
hgdprs879255262
ensemblrs879255262
gopubmedrs879255262
geneviewrs879255262
scholarrs879255262
googlers879255262
pharmgkbrs879255262
gwascentralrs879255262
openSNPrs879255262
23andMers879255262
23andMe allrs879255262
SNP Nexus

SNPshotrs879255262
SNPdbers879255262
MSV3drs879255262
GWAS Ctlgrs879255262
Max Magnitude0
ClinVar
Risk rs879255262(T;T)
Alt rs879255262(T;T)
Reference rs879255262(A;A)
Significance Pathogenic
Disease Hypotrichosis 8
Variation info
Gene RB1 LPAR6
CLNDBN Hypotrichosis 8
Reversed 1
HGVS NC_000013.10:g.48986372T>A
CLNSRC
CLNACC RCV000239380.1,