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rs45501500

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45501500(A;A)
Make rs45501500(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201363390
GeneTNNT2
is asnp
is mentioned by
dbSNPrs45501500
ebirs45501500
HLIrs45501500
Exacrs45501500
Varsomers45501500
Maprs45501500
PheGenIrs45501500
hapmaprs45501500
1000 genomesrs45501500
hgdprs45501500
ensemblrs45501500
gopubmedrs45501500
geneviewrs45501500
scholarrs45501500
googlers45501500
pharmgkbrs45501500
gwascentralrs45501500
openSNPrs45501500
23andMers45501500
23andMe allrs45501500
SNP Nexus

SNPshotrs45501500
SNPdbers45501500
MSV3drs45501500
GWAS Ctlgrs45501500
Max Magnitude0
ClinVar
Risk rs45501500(A;A)
Alt rs45501500(A;A)
Reference rs45501500(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TNNT2
CLNDBN not specified not provided
Reversed 1
HGVS NC_000001.10:g.201332518C>T
CLNSRC
CLNACC RCV000036595.3, RCV000225721.1,