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rs387906386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906386(-;-)
Make rs387906386(-;A)
ReferenceGRCh38 38.1/141
Chromosome1
Position94062666
GeneABCA4
is asnp
is mentioned by
dbSNPrs387906386
ebirs387906386
HLIrs387906386
Exacrs387906386
Varsomers387906386
Maprs387906386
PheGenIrs387906386
hapmaprs387906386
1000 genomesrs387906386
hgdprs387906386
ensemblrs387906386
gopubmedrs387906386
geneviewrs387906386
scholarrs387906386
googlers387906386
pharmgkbrs387906386
gwascentralrs387906386
openSNPrs387906386
23andMers387906386
23andMe allrs387906386
SNP Nexus

SNPshotrs387906386
SNPdbers387906386
MSV3drs387906386
GWAS Ctlgrs387906386
Max Magnitude0
ClinVar
Risk rs387906386(;)
Alt rs387906386(;)
Reference rs387906386(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,