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rs786205447

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205447(G;T)
Make rs786205447(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position94047022
GeneABCA4
is asnp
is mentioned by
dbSNPrs786205447
ebirs786205447
HLIrs786205447
Exacrs786205447
Varsomers786205447
Maprs786205447
PheGenIrs786205447
hapmaprs786205447
1000 genomesrs786205447
hgdprs786205447
ensemblrs786205447
gopubmedrs786205447
geneviewrs786205447
scholarrs786205447
googlers786205447
pharmgkbrs786205447
gwascentralrs786205447
openSNPrs786205447
23andMers786205447
23andMe allrs786205447
SNP Nexus

SNPshotrs786205447
SNPdbers786205447
MSV3drs786205447
GWAS Ctlgrs786205447
Max Magnitude0
ClinVar
Risk rs786205447(T;T)
Alt rs786205447(T;T)
Reference rs786205447(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA4
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.94512578C>A
CLNSRC
CLNACC RCV000171156.1,