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rs752742151

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752742151(C;T)
Make rs752742151(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position130147774
GeneAIFM1
is asnp
is mentioned by
dbSNPrs752742151
ebirs752742151
HLIrs752742151
Exacrs752742151
Varsomers752742151
Maprs752742151
PheGenIrs752742151
hapmaprs752742151
1000 genomesrs752742151
hgdprs752742151
ensemblrs752742151
gopubmedrs752742151
geneviewrs752742151
scholarrs752742151
googlers752742151
pharmgkbrs752742151
gwascentralrs752742151
openSNPrs752742151
23andMers752742151
23andMe allrs752742151
SNP Nexus

SNPshotrs752742151
SNPdbers752742151
MSV3drs752742151
GWAS Ctlgrs752742151
Max Magnitude0
ClinVar
Risk rs752742151(T;T)
Alt rs752742151(T;T)
Reference rs752742151(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AIFM1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.129281749C>T
CLNSRC
CLNACC RCV000196053.1,