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rs876661345

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661345(-;-)
Make rs876661345(-;C)
Make rs876661345(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154379760
GeneEMD
is asnp
is mentioned by
dbSNPrs876661345
ebirs876661345
HLIrs876661345
Exacrs876661345
Varsomers876661345
Maprs876661345
PheGenIrs876661345
hapmaprs876661345
1000 genomesrs876661345
hgdprs876661345
ensemblrs876661345
gopubmedrs876661345
geneviewrs876661345
scholarrs876661345
googlers876661345
pharmgkbrs876661345
gwascentralrs876661345
openSNPrs876661345
23andMers876661345
23andMe allrs876661345
SNP Nexus

SNPshotrs876661345
SNPdbers876661345
MSV3drs876661345
GWAS Ctlgrs876661345
Max Magnitude0
ClinVar
Risk rs876661345(C;C)
Alt rs876661345(C;C)
Reference rs876661345(;)
Significance Pathogenic
Disease not provided
Variation info
Gene EMD
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153608120dupC
CLNSRC
CLNACC RCV000223909.1,