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rs761440783

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761440783(A;A)
Make rs761440783(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position61839540
GeneFAM161A
is asnp
is mentioned by
dbSNPrs761440783
ebirs761440783
HLIrs761440783
Exacrs761440783
Varsomers761440783
Maprs761440783
PheGenIrs761440783
hapmaprs761440783
1000 genomesrs761440783
hgdprs761440783
ensemblrs761440783
gopubmedrs761440783
geneviewrs761440783
scholarrs761440783
googlers761440783
pharmgkbrs761440783
gwascentralrs761440783
openSNPrs761440783
23andMers761440783
23andMe allrs761440783
SNP Nexus

SNPshotrs761440783
SNPdbers761440783
MSV3drs761440783
GWAS Ctlgrs761440783
Max Magnitude0
ClinVar
Risk rs761440783(A;A)
Alt rs761440783(A;A)
Reference rs761440783(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene FAM161A
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000002.11:g.62066675C>T
CLNSRC
CLNACC RCV000225381.1,