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rs115596308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs115596308(A;A)
Make rs115596308(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position48411837
GeneLPAR6, RB1
is asnp
is mentioned by
dbSNPrs115596308
ebirs115596308
HLIrs115596308
Exacrs115596308
Varsomers115596308
Maprs115596308
PheGenIrs115596308
hapmaprs115596308
1000 genomesrs115596308
hgdprs115596308
ensemblrs115596308
gopubmedrs115596308
geneviewrs115596308
scholarrs115596308
googlers115596308
pharmgkbrs115596308
gwascentralrs115596308
openSNPrs115596308
23andMers115596308
23andMe allrs115596308
SNP Nexus

SNPshotrs115596308
SNPdbers115596308
MSV3drs115596308
GWAS Ctlgrs115596308
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs115596308(A,C;A,C)
Alt rs115596308(A,C;A,C)
Reference rs115596308(G;G)
Significance Pathogenic
Disease Hypotrichosis 8
Variation info
Gene RB1 LPAR6
CLNDBN Hypotrichosis 8
Reversed 0
HGVS NC_000013.10:g.48985973G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023760.2,