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rs775146234

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775146234(A;A)
Make rs775146234(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1105814
GeneGPX4
is asnp
is mentioned by
dbSNPrs775146234
ebirs775146234
HLIrs775146234
Exacrs775146234
Varsomers775146234
Maprs775146234
PheGenIrs775146234
hapmaprs775146234
1000 genomesrs775146234
hgdprs775146234
ensemblrs775146234
gopubmedrs775146234
geneviewrs775146234
scholarrs775146234
googlers775146234
pharmgkbrs775146234
gwascentralrs775146234
openSNPrs775146234
23andMers775146234
23andMe allrs775146234
SNP Nexus

SNPshotrs775146234
SNPdbers775146234
MSV3drs775146234
GWAS Ctlgrs775146234
Max Magnitude0
ClinVar
Risk rs775146234(A;A)
Alt rs775146234(A;A)
Reference rs775146234(G;G)
Significance Pathogenic
Disease Spondylometaphyseal dysplasia Sedaghatian type
Variation info
Gene GPX4
CLNDBN Spondylometaphyseal dysplasia Sedaghatian type
Reversed 0
HGVS NC_000019.9:g.1105813G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128831.4,