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rs876657403

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657403(C;T)
Make rs876657403(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position225921254
GenePYCR2
is asnp
is mentioned by
dbSNPrs876657403
ebirs876657403
HLIrs876657403
Exacrs876657403
Varsomers876657403
Maprs876657403
PheGenIrs876657403
hapmaprs876657403
1000 genomesrs876657403
hgdprs876657403
ensemblrs876657403
gopubmedrs876657403
geneviewrs876657403
scholarrs876657403
googlers876657403
pharmgkbrs876657403
gwascentralrs876657403
openSNPrs876657403
23andMers876657403
23andMe allrs876657403
SNP Nexus

SNPshotrs876657403
SNPdbers876657403
MSV3drs876657403
GWAS Ctlgrs876657403
Max Magnitude0
ClinVar
Risk rs876657403(T;T)
Alt rs876657403(T;T)
Reference rs876657403(C;C)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene PYCR2
CLNDBN Leukodystrophy, hypomyelinating, 10
Reversed 1
HGVS NC_000001.10:g.226108954G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000173022.2,