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rs730881063

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881063(A;T)
Make rs730881063(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position52454008
GeneNISCH, TNNC1
is asnp
is mentioned by
dbSNPrs730881063
ebirs730881063
HLIrs730881063
Exacrs730881063
Varsomers730881063
Maprs730881063
PheGenIrs730881063
hapmaprs730881063
1000 genomesrs730881063
hgdprs730881063
ensemblrs730881063
gopubmedrs730881063
geneviewrs730881063
scholarrs730881063
googlers730881063
pharmgkbrs730881063
gwascentralrs730881063
openSNPrs730881063
23andMers730881063
23andMe allrs730881063
SNP Nexus

SNPshotrs730881063
SNPdbers730881063
MSV3drs730881063
GWAS Ctlgrs730881063
Max Magnitude0
ClinVar
Risk rs730881063(T;T)
Alt rs730881063(T;T)
Reference rs730881063(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNC1 NISCH
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.52488024T>A
CLNSRC
CLNACC RCV000159203.2,