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

rs318240757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs318240757(A;T)
Make rs318240757(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position70135273
GeneRTTN
is asnp
is mentioned by
dbSNPrs318240757
ebirs318240757
HLIrs318240757
Exacrs318240757
Varsomers318240757
Maprs318240757
PheGenIrs318240757
hapmaprs318240757
1000 genomesrs318240757
hgdprs318240757
ensemblrs318240757
gopubmedrs318240757
geneviewrs318240757
scholarrs318240757
googlers318240757
pharmgkbrs318240757
gwascentralrs318240757
openSNPrs318240757
23andMers318240757
23andMe allrs318240757
SNP Nexus

SNPshotrs318240757
SNPdbers318240757
MSV3drs318240757
GWAS Ctlgrs318240757
Max Magnitude0
ClinVar
Risk rs318240757(T;T)
Alt rs318240757(T;T)
Reference rs318240757(A;A)
Significance Pathogenic
Disease MICROCEPHALY not provided
Variation info
Gene RTTN
CLNDBN MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES not provided
Reversed 1
HGVS NC_000018.9:g.67802509T>A
CLNSRC OMIM Allelic Variant UniProtKB (variants)
CLNACC RCV000030785.3, RCV000059810.1,