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rs775277800

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775277800(C;T)
Make rs775277800(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position70166989
GeneRTTN
is asnp
is mentioned by
dbSNPrs775277800
ebirs775277800
HLIrs775277800
Exacrs775277800
Varsomers775277800
Maprs775277800
PheGenIrs775277800
hapmaprs775277800
1000 genomesrs775277800
hgdprs775277800
ensemblrs775277800
gopubmedrs775277800
geneviewrs775277800
scholarrs775277800
googlers775277800
pharmgkbrs775277800
gwascentralrs775277800
openSNPrs775277800
23andMers775277800
23andMe allrs775277800
SNP Nexus

SNPshotrs775277800
SNPdbers775277800
MSV3drs775277800
GWAS Ctlgrs775277800
Max Magnitude0
ClinVar
Risk rs775277800(T;T)
Alt rs775277800(T;T)
Reference rs775277800(C;C)
Significance Pathogenic
Disease Congenital microcephaly Microcephaly
Variation info
Gene RTTN
CLNDBN Congenital microcephaly Microcephaly, short stature, and polymicrogyria with or without seizures
Reversed 0
HGVS NC_000018.9:g.67834225C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000203569.1, RCV000210338.1,