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rs781995242

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781995242(A;A)
Make rs781995242(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position78029290
GeneATP7A
is asnp
is mentioned by
dbSNPrs781995242
ebirs781995242
HLIrs781995242
Exacrs781995242
Varsomers781995242
Maprs781995242
PheGenIrs781995242
hapmaprs781995242
1000 genomesrs781995242
hgdprs781995242
ensemblrs781995242
gopubmedrs781995242
geneviewrs781995242
scholarrs781995242
googlers781995242
pharmgkbrs781995242
gwascentralrs781995242
openSNPrs781995242
23andMers781995242
23andMe allrs781995242
SNP Nexus

SNPshotrs781995242
SNPdbers781995242
MSV3drs781995242
GWAS Ctlgrs781995242
Max Magnitude0
ClinVar
Risk rs781995242(A;A)
Alt rs781995242(A;A)
Reference rs781995242(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP7A
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.77284787G>A
CLNSRC
CLNACC RCV000235979.1,