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rs766773277

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766773277(A;A)
Make rs766773277(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74524723
GeneSLC16A2
is asnp
is mentioned by
dbSNPrs766773277
ebirs766773277
HLIrs766773277
Exacrs766773277
Varsomers766773277
Maprs766773277
PheGenIrs766773277
hapmaprs766773277
1000 genomesrs766773277
hgdprs766773277
ensemblrs766773277
gopubmedrs766773277
geneviewrs766773277
scholarrs766773277
googlers766773277
pharmgkbrs766773277
gwascentralrs766773277
openSNPrs766773277
23andMers766773277
23andMe allrs766773277
SNP Nexus

SNPshotrs766773277
SNPdbers766773277
MSV3drs766773277
GWAS Ctlgrs766773277
Max Magnitude0
ClinVar
Risk rs766773277(A;A)
Alt rs766773277(A;A)
Reference rs766773277(C;C)
Significance Pathogenic
Disease Allan-Herndon-Dudley syndrome
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome
Reversed 0
HGVS NC_000023.10:g.73744558C>T
CLNSRC
CLNACC RCV000193469.1,