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rs150936840

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150936840(C;T)
Make rs150936840(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position123707995
GeneLOC105369194, MYLK
is asnp
is mentioned by
dbSNPrs150936840
ebirs150936840
HLIrs150936840
Exacrs150936840
Varsomers150936840
Maprs150936840
PheGenIrs150936840
hapmaprs150936840
1000 genomesrs150936840
hgdprs150936840
ensemblrs150936840
gopubmedrs150936840
geneviewrs150936840
scholarrs150936840
googlers150936840
pharmgkbrs150936840
gwascentralrs150936840
openSNPrs150936840
23andMers150936840
23andMe allrs150936840
SNP Nexus

SNPshotrs150936840
SNPdbers150936840
MSV3drs150936840
GWAS Ctlgrs150936840
Max Magnitude0
ClinVar
Risk rs150936840(A,T;A,T)
Alt rs150936840(A,T;A,T)
Reference rs150936840(C;C)
Significance Probable-Pathogenic
Disease Aortic aneurysm
Variation info
Gene MYLK LOC101927028
CLNDBN Aortic aneurysm, familial thoracic 7
Reversed 0
HGVS NC_000003.11:g.123426842C>A
CLNSRC
CLNACC RCV000198643.1,