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rs797044691

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044691(-;A)
Make rs797044691(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position70127504
GeneRTTN
is asnp
is mentioned by
dbSNPrs797044691
ClinGenrs797044691
ebirs797044691
HLIrs797044691
Exacrs797044691
Varsomers797044691
Maprs797044691
PheGenIrs797044691
hapmaprs797044691
1000 genomesrs797044691
hgdprs797044691
ensemblrs797044691
gopubmedrs797044691
geneviewrs797044691
scholarrs797044691
googlers797044691
pharmgkbrs797044691
gwascentralrs797044691
openSNPrs797044691
23andMers797044691
23andMe allrs797044691
SNP Nexus

SNPshotrs797044691
SNPdbers797044691
MSV3drs797044691
GWAS Ctlgrs797044691
Max Magnitude0
ClinVar
Risk rs797044691(A;A)
Alt rs797044691(A;A)
Reference Rs797044691(;)
Significance Probable-Pathogenic
Disease Microcephaly
Variation info
Gene RTTN
CLNDBN Microcephaly, short stature, and polymicrogyria with or without seizures
Reversed 1
HGVS NC_000018.9:g.67794741dupT
CLNSRC
CLNACC RCV000176596.1,