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rs771055145

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs771055145(A;G)
Make rs771055145(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position12704577
GeneLURAP1L-AS1, TYRP1
is asnp
is mentioned by
dbSNPrs771055145
dbSNP (classic)rs771055145
ClinGenrs771055145
ebirs771055145
HLIrs771055145
Exacrs771055145
Gnomadrs771055145
Varsomers771055145
LitVarrs771055145
Maprs771055145
PheGenIrs771055145
Biobankrs771055145
1000 genomesrs771055145
hgdprs771055145
ensemblrs771055145
geneviewrs771055145
scholarrs771055145
googlers771055145
pharmgkbrs771055145
gwascentralrs771055145
openSNPrs771055145
23andMers771055145
SNPshotrs771055145
SNPdbers771055145
MSV3drs771055145
GWAS Ctlgrs771055145
Max Magnitude0
ClinVar
Risk rs771055145(G;G)
Alt rs771055145(G;G)
Reference Rs771055145(A;A)
Significance Probable-Pathogenic
Disease Ocular albinism
Variation info
Gene TYRP1 LURAP1L-AS1
CLNDBN Ocular albinism
Reversed 0
HGVS NC_000009.11:g.12704577A>G
CLNSRC
CLNACC RCV000414933.1,