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rs864321620

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321620(A;G)
Make rs864321620(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position70135176
GeneRTTN
is asnp
is mentioned by
dbSNPrs864321620
ebirs864321620
HLIrs864321620
Exacrs864321620
Varsomers864321620
Maprs864321620
PheGenIrs864321620
hapmaprs864321620
1000 genomesrs864321620
hgdprs864321620
ensemblrs864321620
gopubmedrs864321620
geneviewrs864321620
scholarrs864321620
googlers864321620
pharmgkbrs864321620
gwascentralrs864321620
openSNPrs864321620
23andMers864321620
23andMe allrs864321620
SNP Nexus

SNPshotrs864321620
SNPdbers864321620
MSV3drs864321620
GWAS Ctlgrs864321620
Max Magnitude0
ClinVar
Risk rs864321620(G;G)
Alt rs864321620(G;G)
Reference rs864321620(A;A)
Significance Pathogenic
Disease Congenital microcephaly Microcephaly
Variation info
Gene RTTN
CLNDBN Congenital microcephaly Microcephaly, short stature, and polymicrogyria with or without seizures
Reversed 1
HGVS NC_000018.9:g.67802412T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000203563.1, RCV000210341.1,