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rs727503809

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503809(A;A)
Make rs727503809(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position78885782
GeneARSB
is asnp
is mentioned by
dbSNPrs727503809
ebirs727503809
HLIrs727503809
Exacrs727503809
Varsomers727503809
Maprs727503809
PheGenIrs727503809
hapmaprs727503809
1000 genomesrs727503809
hgdprs727503809
ensemblrs727503809
gopubmedrs727503809
geneviewrs727503809
scholarrs727503809
googlers727503809
pharmgkbrs727503809
gwascentralrs727503809
openSNPrs727503809
23andMers727503809
23andMe allrs727503809
SNP Nexus

SNPshotrs727503809
SNPdbers727503809
MSV3drs727503809
GWAS Ctlgrs727503809
Max Magnitude0
ClinVar
Risk rs727503809(A;A)
Alt rs727503809(A;A)
Reference rs727503809(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARSB
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.78181605C>T
CLNSRC HGMD
CLNACC RCV000152796.3,