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rs864622784

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622784(C;T)
Make rs864622784(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49856402
GeneTRAIP
is asnp
is mentioned by
dbSNPrs864622784
ebirs864622784
HLIrs864622784
Exacrs864622784
Varsomers864622784
Maprs864622784
PheGenIrs864622784
hapmaprs864622784
1000 genomesrs864622784
hgdprs864622784
ensemblrs864622784
gopubmedrs864622784
geneviewrs864622784
scholarrs864622784
googlers864622784
pharmgkbrs864622784
gwascentralrs864622784
openSNPrs864622784
23andMers864622784
23andMe allrs864622784
SNP Nexus

SNPshotrs864622784
SNPdbers864622784
MSV3drs864622784
GWAS Ctlgrs864622784
Max Magnitude0
ClinVar
Risk rs864622784(T;T)
Alt rs864622784(T;T)
Reference rs864622784(C;C)
Significance Pathogenic
Disease Seckel syndrome 9
Variation info
Gene TRAIP
CLNDBN Seckel syndrome 9
Reversed 1
HGVS NC_000003.11:g.49893835G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000206906.1,