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rs112005636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs112005636(A;G)
Make rs112005636(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position93996107
GeneABCA4
is asnp
is mentioned by
dbSNPrs112005636
dbSNP (old)rs112005636
ClinGenrs112005636
ebirs112005636
HLIrs112005636
Exacrs112005636
Gnomadrs112005636
Varsomers112005636
Maprs112005636
PheGenIrs112005636
Biobankrs112005636
1000 genomesrs112005636
hgdprs112005636
ensemblrs112005636
gopubmedrs112005636
geneviewrs112005636
scholarrs112005636
googlers112005636
pharmgkbrs112005636
gwascentralrs112005636
openSNPrs112005636
23andMers112005636
23andMe allrs112005636
SNPshotrs112005636
SNPdbers112005636
MSV3drs112005636
GWAS Ctlgrs112005636
Max Magnitude0
ClinVar
Risk rs112005636(G;G) rs112005636(T;T)
Alt rs112005636(G;G) rs112005636(T;T)
Reference Rs112005636(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA4
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.94461663A>T
CLNSRC
CLNACC RCV000487635.1,