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rs727503786

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503786(C;G)
Make rs727503786(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position153736231
GeneABCD1
is asnp
is mentioned by
dbSNPrs727503786
ebirs727503786
HLIrs727503786
Exacrs727503786
Varsomers727503786
Maprs727503786
PheGenIrs727503786
hapmaprs727503786
1000 genomesrs727503786
hgdprs727503786
ensemblrs727503786
gopubmedrs727503786
geneviewrs727503786
scholarrs727503786
googlers727503786
pharmgkbrs727503786
gwascentralrs727503786
openSNPrs727503786
23andMers727503786
23andMe allrs727503786
SNP Nexus

SNPshotrs727503786
SNPdbers727503786
MSV3drs727503786
GWAS Ctlgrs727503786
Max Magnitude0
ClinVar
Risk rs727503786(A,G;A,G)
Alt rs727503786(A,G;A,G)
Reference rs727503786(C;C)
Significance Probable-Pathogenic
Disease Adrenoleukodystrophy
Variation info
Gene ABCD1
CLNDBN Adrenoleukodystrophy
Reversed 0
HGVS NC_000023.10:g.153001685C>G
CLNSRC HGMD
CLNACC RCV000152719.3,