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rs61751386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61751386(-;-)
Make rs61751386(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position94062667
GeneABCA4
is asnp
is mentioned by
dbSNPrs61751386
ebirs61751386
HLIrs61751386
Exacrs61751386
Varsomers61751386
Maprs61751386
PheGenIrs61751386
hapmaprs61751386
1000 genomesrs61751386
hgdprs61751386
ensemblrs61751386
gopubmedrs61751386
geneviewrs61751386
scholarrs61751386
googlers61751386
pharmgkbrs61751386
gwascentralrs61751386
openSNPrs61751386
23andMers61751386
23andMe allrs61751386
SNP Nexus

SNPshotrs61751386
SNPdbers61751386
MSV3drs61751386
GWAS Ctlgrs61751386
Max Magnitude0
ClinVar
Risk rs61751386(;)
Alt rs61751386(;)
Reference rs61751386(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 19 not provided
Variation info
Gene ABCA4
CLNDBN Retinitis pigmentosa 19 not provided
Reversed 1
HGVS NC_000001.10:g.94528222delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000008342.3, RCV000085435.1,