Have questions? Visit https://www.reddit.com/r/SNPedia

rs200361128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200361128(C;G)
Make rs200361128(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position140504904
GeneSOX3
is asnp
is mentioned by
dbSNPrs200361128
dbSNP (old)rs200361128
ClinGenrs200361128
ebirs200361128
HLIrs200361128
Exacrs200361128
Gnomadrs200361128
Varsomers200361128
LitVarrs200361128
Maprs200361128
PheGenIrs200361128
Biobankrs200361128
1000 genomesrs200361128
hgdprs200361128
ensemblrs200361128
gopubmedrs200361128
geneviewrs200361128
scholarrs200361128
googlers200361128
pharmgkbrs200361128
gwascentralrs200361128
openSNPrs200361128
23andMers200361128
23andMe allrs200361128
SNPshotrs200361128
SNPdbers200361128
MSV3drs200361128
GWAS Ctlgrs200361128
Max Magnitude0
ClinVar
Risk rs200361128(G;G)
Alt rs200361128(G;G)
Reference Rs200361128(C;C)
Significance Probable-Pathogenic
Disease not specified Abnormality of brain morphology
Variation info
Gene SOX3
CLNDBN not specified Abnormality of brain morphology
Reversed 0
HGVS NC_000023.10:g.139587069C>G
CLNSRC
CLNACC RCV000153990.3, RCV000454344.1,