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rs767664526

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767664526(A;A)
Make rs767664526(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49841890
GeneTRAIP
is asnp
is mentioned by
dbSNPrs767664526
ClinGenrs767664526
ebirs767664526
HLIrs767664526
Exacrs767664526
Varsomers767664526
Maprs767664526
PheGenIrs767664526
hapmaprs767664526
1000 genomesrs767664526
hgdprs767664526
ensemblrs767664526
gopubmedrs767664526
geneviewrs767664526
scholarrs767664526
googlers767664526
pharmgkbrs767664526
gwascentralrs767664526
openSNPrs767664526
23andMers767664526
23andMe allrs767664526
SNP Nexus

SNPshotrs767664526
SNPdbers767664526
MSV3drs767664526
GWAS Ctlgrs767664526
Max Magnitude0
ClinVar
Risk rs767664526(A;A)
Alt rs767664526(A;A)
Reference Rs767664526(G;G)
Significance Pathogenic
Disease Seckel syndrome 9
Variation info
Gene TRAIP
CLNDBN Seckel syndrome 9
Reversed 0
HGVS NC_000003.11:g.49879323G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000206973.1,