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rs369082457

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369082457(C;T)
Make rs369082457(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position39184951
GeneXIRP1
is asnp
is mentioned by
dbSNPrs369082457
ebirs369082457
HLIrs369082457
Exacrs369082457
Varsomers369082457
Maprs369082457
PheGenIrs369082457
hapmaprs369082457
1000 genomesrs369082457
hgdprs369082457
ensemblrs369082457
gopubmedrs369082457
geneviewrs369082457
scholarrs369082457
googlers369082457
pharmgkbrs369082457
gwascentralrs369082457
openSNPrs369082457
23andMers369082457
23andMe allrs369082457
SNP Nexus

SNPshotrs369082457
SNPdbers369082457
MSV3drs369082457
GWAS Ctlgrs369082457
Max Magnitude0
ClinVar
Risk rs369082457(T;T)
Alt rs369082457(T;T)
Reference rs369082457(C;C)
Significance Probable-Pathogenic
Disease Classical primary microcephaly
Variation info
Gene XIRP1
CLNDBN Classical primary microcephaly
Reversed 0
HGVS NC_000003.11:g.39226442C>T
CLNSRC
CLNACC RCV000162178.1,