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rs370840449

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370840449(A;A)
Make rs370840449(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154380807
GeneEMD
is asnp
is mentioned by
dbSNPrs370840449
ebirs370840449
HLIrs370840449
Exacrs370840449
Varsomers370840449
Maprs370840449
PheGenIrs370840449
hapmaprs370840449
1000 genomesrs370840449
hgdprs370840449
ensemblrs370840449
gopubmedrs370840449
geneviewrs370840449
scholarrs370840449
googlers370840449
pharmgkbrs370840449
gwascentralrs370840449
openSNPrs370840449
23andMers370840449
23andMe allrs370840449
SNP Nexus

SNPshotrs370840449
SNPdbers370840449
MSV3drs370840449
GWAS Ctlgrs370840449
Max Magnitude0
ClinVar
Risk rs370840449(A;A)
Alt rs370840449(A;A)
Reference rs370840449(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EMD
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153609167G>A
CLNSRC
CLNACC RCV000183442.2,