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rs200967229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a mutation for Stargardt disease
Make rs200967229(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position94030427
GeneABCA4
is asnp
is mentioned by
dbSNPrs200967229
dbSNP (classic)rs200967229
ClinGenrs200967229
ebirs200967229
HLIrs200967229
Exacrs200967229
Gnomadrs200967229
Varsomers200967229
LitVarrs200967229
Maprs200967229
PheGenIrs200967229
Biobankrs200967229
1000 genomesrs200967229
hgdprs200967229
ensemblrs200967229
geneviewrs200967229
scholarrs200967229
googlers200967229
pharmgkbrs200967229
gwascentralrs200967229
openSNPrs200967229
23andMers200967229
SNPshotrs200967229
SNPdbers200967229
MSV3drs200967229
GWAS Ctlgrs200967229
Max Magnitude3
ClinVar
Risk rs200967229(T;T)
Alt rs200967229(T;T)
Reference Rs200967229(C;C)
Significance Pathogenic
Disease Stargardt disease 1
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1
Reversed 0
HGVS NC_000001.10:g.94495983C>T
CLNSRC
CLNACC RCV000408571.1,