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rs763722868

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763722868(C;C)
Make rs763722868(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178775572
GeneLOC101927055, TTN
is asnp
is mentioned by
dbSNPrs763722868
ebirs763722868
HLIrs763722868
Exacrs763722868
Varsomers763722868
Maprs763722868
PheGenIrs763722868
hapmaprs763722868
1000 genomesrs763722868
hgdprs763722868
ensemblrs763722868
gopubmedrs763722868
geneviewrs763722868
scholarrs763722868
googlers763722868
pharmgkbrs763722868
gwascentralrs763722868
openSNPrs763722868
23andMers763722868
23andMe allrs763722868
SNP Nexus

SNPshotrs763722868
SNPdbers763722868
MSV3drs763722868
GWAS Ctlgrs763722868
Max Magnitude0
ClinVar
Risk rs763722868(A,C;A,C)
Alt rs763722868(A,C;A,C)
Reference rs763722868(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN LOC101927055
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179640299G>C
CLNSRC
CLNACC RCV000171325.1,