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rs786205446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205446(A;A)
Make rs786205446(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position94021406
GeneABCA4
is asnp
is mentioned by
dbSNPrs786205446
dbSNP (old)rs786205446
ClinGenrs786205446
ebirs786205446
HLIrs786205446
Exacrs786205446
Varsomers786205446
Maprs786205446
PheGenIrs786205446
Biobankrs786205446
1000 genomesrs786205446
hgdprs786205446
ensemblrs786205446
gopubmedrs786205446
geneviewrs786205446
scholarrs786205446
googlers786205446
pharmgkbrs786205446
gwascentralrs786205446
openSNPrs786205446
23andMers786205446
23andMe allrs786205446
SNP Nexus

SNPshotrs786205446
SNPdbers786205446
MSV3drs786205446
GWAS Ctlgrs786205446
Max Magnitude0
ClinVar
Risk rs786205446(A;A)
Alt rs786205446(A;A)
Reference Rs786205446(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA4
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.94486962A>T
CLNSRC
CLNACC RCV000171155.1,