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rs748155949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748155949(C;C)
Make rs748155949(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position88731721
GeneLOC100289580, PIEZO1
is asnp
is mentioned by
dbSNPrs748155949
dbSNP (classic)rs748155949
ClinGenrs748155949
ebirs748155949
HLIrs748155949
Exacrs748155949
Gnomadrs748155949
Varsomers748155949
LitVarrs748155949
Maprs748155949
PheGenIrs748155949
Biobankrs748155949
1000 genomesrs748155949
hgdprs748155949
ensemblrs748155949
geneviewrs748155949
scholarrs748155949
googlers748155949
pharmgkbrs748155949
gwascentralrs748155949
openSNPrs748155949
23andMers748155949
SNPshotrs748155949
SNPdbers748155949
MSV3drs748155949
GWAS Ctlgrs748155949
Max Magnitude0
ClinVar
Risk rs748155949(C;C)
Alt rs748155949(C;C)
Reference Rs748155949(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC100289580 PIEZO1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.88798129G>C
CLNSRC
CLNACC RCV000490090.1,