Have questions? Visit https://www.reddit.com/r/SNPedia

rs372781135

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372781135(A;A)
Make rs372781135(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position225922043
GeneMIR6741, PYCR2
is asnp
is mentioned by
dbSNPrs372781135
ebirs372781135
HLIrs372781135
Exacrs372781135
Varsomers372781135
Maprs372781135
PheGenIrs372781135
hapmaprs372781135
1000 genomesrs372781135
hgdprs372781135
ensemblrs372781135
gopubmedrs372781135
geneviewrs372781135
scholarrs372781135
googlers372781135
pharmgkbrs372781135
gwascentralrs372781135
openSNPrs372781135
23andMers372781135
23andMe allrs372781135
SNP Nexus

SNPshotrs372781135
SNPdbers372781135
MSV3drs372781135
GWAS Ctlgrs372781135
Max Magnitude0
ClinVar
Risk rs372781135(A;A)
Alt rs372781135(A;A)
Reference rs372781135(G;G)
Significance Pathogenic
Disease Leukodystrophy
Variation info
Gene PYCR2 MIR6741
CLNDBN Leukodystrophy, hypomyelinating, 10
Reversed 0
HGVS NC_000001.10:g.226109743G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000173021.2,