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rs141823837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141823837(C;T)
Make rs141823837(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position94060739
GeneABCA4
is asnp
is mentioned by
dbSNPrs141823837
dbSNP (classic)rs141823837
ClinGenrs141823837
ebirs141823837
HLIrs141823837
Exacrs141823837
Gnomadrs141823837
Varsomers141823837
LitVarrs141823837
Maprs141823837
PheGenIrs141823837
Biobankrs141823837
1000 genomesrs141823837
hgdprs141823837
ensemblrs141823837
geneviewrs141823837
scholarrs141823837
googlers141823837
pharmgkbrs141823837
gwascentralrs141823837
openSNPrs141823837
23andMers141823837
SNPshotrs141823837
SNPdbers141823837
MSV3drs141823837
GWAS Ctlgrs141823837
Max Magnitude0
ClinVar
Risk rs141823837(T;T)
Alt rs141823837(T;T)
Reference Rs141823837(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA4
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.94526295C>T
CLNSRC
CLNACC RCV000484928.1,