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rs606231254

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231254(C;C)
Make rs606231254(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position38780924
GeneDNAL4
is asnp
is mentioned by
dbSNPrs606231254
ebirs606231254
HLIrs606231254
Exacrs606231254
Varsomers606231254
Maprs606231254
PheGenIrs606231254
hapmaprs606231254
1000 genomesrs606231254
hgdprs606231254
ensemblrs606231254
gopubmedrs606231254
geneviewrs606231254
scholarrs606231254
googlers606231254
pharmgkbrs606231254
gwascentralrs606231254
openSNPrs606231254
23andMers606231254
23andMe allrs606231254
SNP Nexus

SNPshotrs606231254
SNPdbers606231254
MSV3drs606231254
GWAS Ctlgrs606231254
Max Magnitude0
ClinVar
Risk rs606231254(C;C)
Alt rs606231254(C;C)
Reference rs606231254(T;T)
Significance Pathogenic
Disease Mirror movements 3
Variation info
Gene DNAL4
CLNDBN Mirror movements 3
Reversed 1
HGVS NC_000022.10:g.39176929A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144852.3,