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rs755769516

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs755769516(C;T)
Make rs755769516(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position136743693
GeneARHGEF6
is asnp
is mentioned by
dbSNPrs755769516
ebirs755769516
HLIrs755769516
Exacrs755769516
Varsomers755769516
Maprs755769516
PheGenIrs755769516
hapmaprs755769516
1000 genomesrs755769516
hgdprs755769516
ensemblrs755769516
gopubmedrs755769516
geneviewrs755769516
scholarrs755769516
googlers755769516
pharmgkbrs755769516
gwascentralrs755769516
openSNPrs755769516
23andMers755769516
23andMe allrs755769516
SNP Nexus

SNPshotrs755769516
SNPdbers755769516
MSV3drs755769516
GWAS Ctlgrs755769516
Max Magnitude0
ClinVar
Risk rs755769516(T;T)
Alt rs755769516(T;T)
Reference rs755769516(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARHGEF6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135825852C>T
CLNSRC
CLNACC RCV000171446.1,