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rs727504028

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504028(G;T)
Make rs727504028(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position42536656
GeneNAGLU
is asnp
is mentioned by
dbSNPrs727504028
ebirs727504028
HLIrs727504028
Exacrs727504028
Varsomers727504028
Maprs727504028
PheGenIrs727504028
hapmaprs727504028
1000 genomesrs727504028
hgdprs727504028
ensemblrs727504028
gopubmedrs727504028
geneviewrs727504028
scholarrs727504028
googlers727504028
pharmgkbrs727504028
gwascentralrs727504028
openSNPrs727504028
23andMers727504028
23andMe allrs727504028
SNP Nexus

SNPshotrs727504028
SNPdbers727504028
MSV3drs727504028
GWAS Ctlgrs727504028
Max Magnitude0
ClinVar
Risk rs727504028(T;T)
Alt rs727504028(T;T)
Reference rs727504028(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NAGLU
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.40688674G>T
CLNSRC
CLNACC RCV000153531.3,