Have questions? Visit https://www.reddit.com/r/SNPedia

rs768431507

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768431507(A;A)
Make rs768431507(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178605011
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs768431507
ebirs768431507
HLIrs768431507
Exacrs768431507
Varsomers768431507
Maprs768431507
PheGenIrs768431507
hapmaprs768431507
1000 genomesrs768431507
hgdprs768431507
ensemblrs768431507
gopubmedrs768431507
geneviewrs768431507
scholarrs768431507
googlers768431507
pharmgkbrs768431507
gwascentralrs768431507
openSNPrs768431507
23andMers768431507
23andMe allrs768431507
SNP Nexus

SNPshotrs768431507
SNPdbers768431507
MSV3drs768431507
GWAS Ctlgrs768431507
Max Magnitude0
ClinVar
Risk rs768431507(A;A)
Alt rs768431507(A;A)
Reference rs768431507(G;G)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene TTN TTN-AS1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000002.11:g.179469738G>A
CLNSRC
CLNACC RCV000184378.2, RCV000223808.1,