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rs1012472070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1012472070(G;T)
Make rs1012472070(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position88738367
GeneLOC100289580, PIEZO1
is asnp
is mentioned by
dbSNPrs1012472070
dbSNP (old)rs1012472070
ClinGenrs1012472070
ebirs1012472070
HLIrs1012472070
Exacrs1012472070
Gnomadrs1012472070
Varsomers1012472070
LitVarrs1012472070
Maprs1012472070
PheGenIrs1012472070
Biobankrs1012472070
1000 genomesrs1012472070
hgdprs1012472070
ensemblrs1012472070
gopubmedrs1012472070
geneviewrs1012472070
scholarrs1012472070
googlers1012472070
pharmgkbrs1012472070
gwascentralrs1012472070
openSNPrs1012472070
23andMers1012472070
23andMe allrs1012472070
SNPshotrs1012472070
SNPdbers1012472070
MSV3drs1012472070
GWAS Ctlgrs1012472070
Max Magnitude0
ClinVar
Risk rs1012472070(A;A) rs1012472070(T;T)
Alt rs1012472070(A;A) rs1012472070(T;T)
Reference Rs1012472070(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.88804775G>T
CLNSRC
CLNACC RCV000479073.1,