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rs786205445

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786205445(-;-)
Make rs786205445(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position94014611
GeneABCA4
is asnp
is mentioned by
dbSNPrs786205445
ebirs786205445
HLIrs786205445
Exacrs786205445
Varsomers786205445
Maprs786205445
PheGenIrs786205445
hapmaprs786205445
1000 genomesrs786205445
hgdprs786205445
ensemblrs786205445
gopubmedrs786205445
geneviewrs786205445
scholarrs786205445
googlers786205445
pharmgkbrs786205445
gwascentralrs786205445
openSNPrs786205445
23andMers786205445
23andMe allrs786205445
SNP Nexus

SNPshotrs786205445
SNPdbers786205445
MSV3drs786205445
GWAS Ctlgrs786205445
Max Magnitude0
ClinVar
Risk rs786205445(;)
Alt rs786205445(;)
Reference rs786205445(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA4
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.94480167_94480168delCA
CLNSRC
CLNACC RCV000171154.1,