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rs200544616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200544616(G;T)
Make rs200544616(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position112646956
GeneLARP7
is asnp
is mentioned by
dbSNPrs200544616
dbSNP (old)rs200544616
ClinGenrs200544616
ebirs200544616
HLIrs200544616
Exacrs200544616
Gnomadrs200544616
Varsomers200544616
LitVarrs200544616
Maprs200544616
PheGenIrs200544616
Biobankrs200544616
1000 genomesrs200544616
hgdprs200544616
ensemblrs200544616
gopubmedrs200544616
geneviewrs200544616
scholarrs200544616
googlers200544616
pharmgkbrs200544616
gwascentralrs200544616
openSNPrs200544616
23andMers200544616
23andMe allrs200544616
SNPshotrs200544616
SNPdbers200544616
MSV3drs200544616
GWAS Ctlgrs200544616
Max Magnitude0
ClinVar
Risk rs200544616(T;T)
Alt rs200544616(T;T)
Reference Rs200544616(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LARP7
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.113568112G>T
CLNSRC
CLNACC RCV000426555.1,