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rs61753190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0
(CAT;CAT) 0 common in clinvar
(I;I) 0
Make rs61753190(-;A)
Make rs61753190(A;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position89178239
GeneTYR
is asnp
is mentioned by
dbSNPrs61753190
ebirs61753190
HLIrs61753190
Exacrs61753190
Varsomers61753190
Maprs61753190
PheGenIrs61753190
hapmaprs61753190
1000 genomesrs61753190
hgdprs61753190
ensemblrs61753190
gopubmedrs61753190
geneviewrs61753190
scholarrs61753190
googlers61753190
pharmgkbrs61753190
gwascentralrs61753190
openSNPrs61753190
23andMers61753190
23andMe allrs61753190
SNP Nexus

SNPshotrs61753190
SNPdbers61753190
MSV3drs61753190
GWAS Ctlgrs61753190
Max Magnitude0
OMIM606933
Desc
Variant0018
Relatedalso


ClinVar
Risk rs61753190(A;A)
Alt rs61753190(A;A)
Reference rs61753190(CAT;CAT)
Significance Pathogenic
Disease Tyrosinase-negative oculocutaneous albinism not provided
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism not provided
Reversed 0
HGVS NC_000011.9:g.88911407dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000003991.2, RCV000085942.1,