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rs144337183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144337183(A;A)
Make rs144337183(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position41869748
GeneMIR6797, RPS19
is asnp
is mentioned by
dbSNPrs144337183
dbSNP (classic)rs144337183
ClinGenrs144337183
ebirs144337183
HLIrs144337183
Exacrs144337183
Gnomadrs144337183
Varsomers144337183
LitVarrs144337183
Maprs144337183
PheGenIrs144337183
Biobankrs144337183
1000 genomesrs144337183
hgdprs144337183
ensemblrs144337183
geneviewrs144337183
scholarrs144337183
googlers144337183
pharmgkbrs144337183
gwascentralrs144337183
openSNPrs144337183
23andMers144337183
23andMe allrs144337183
SNPshotrs144337183
SNPdbers144337183
MSV3drs144337183
GWAS Ctlgrs144337183
Max Magnitude0
ClinVar
Risk rs144337183(A;A) rs144337183(T;T)
Alt rs144337183(A;A) rs144337183(T;T)
Reference Rs144337183(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR6797 RPS19
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.42373818G>T
CLNSRC
CLNACC RCV000414046.1,