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rs137954284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137954284(C;T)
Make rs137954284(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position216250989
GeneUSH2A
is asnp
is mentioned by
dbSNPrs137954284
dbSNP (classic)rs137954284
ClinGenrs137954284
ebirs137954284
HLIrs137954284
Exacrs137954284
Gnomadrs137954284
Varsomers137954284
LitVarrs137954284
Maprs137954284
PheGenIrs137954284
Biobankrs137954284
1000 genomesrs137954284
hgdprs137954284
ensemblrs137954284
geneviewrs137954284
scholarrs137954284
googlers137954284
pharmgkbrs137954284
gwascentralrs137954284
openSNPrs137954284
23andMers137954284
23andMe allrs137954284
SNPshotrs137954284
SNPdbers137954284
MSV3drs137954284
GWAS Ctlgrs137954284
Max Magnitude0
ClinVar
Risk rs137954284(T;T)
Alt rs137954284(T;T)
Reference Rs137954284(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.216424331C>T
CLNSRC
CLNACC RCV000480360.1,