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rs28938168

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28938168(A;A)
Make rs28938168(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117822424
GeneFXYD2, FXYD6-FXYD2
is asnp
is mentioned by
dbSNPrs28938168
ebirs28938168
HLIrs28938168
Exacrs28938168
Varsomers28938168
Maprs28938168
PheGenIrs28938168
hapmaprs28938168
1000 genomesrs28938168
hgdprs28938168
ensemblrs28938168
gopubmedrs28938168
geneviewrs28938168
scholarrs28938168
googlers28938168
pharmgkbrs28938168
gwascentralrs28938168
openSNPrs28938168
23andMers28938168
23andMe allrs28938168
SNP Nexus

SNPshotrs28938168
SNPdbers28938168
MSV3drs28938168
GWAS Ctlgrs28938168
Max Magnitude0
OMIM601814
DescHYPOMAGNESEMIA 2, RENAL
Variant0001
Relatedalso
ClinVar
Risk rs28938168(A;A)
Alt rs28938168(A;A)
Reference rs28938168(G;G)
Significance Pathogenic
Disease Hypomagnesemia 2
Variation info
Gene FXYD2 FXYD6-FXYD2
CLNDBN Hypomagnesemia 2, renal
Reversed 1
HGVS NC_000011.9:g.117693139C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008123.3,