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rs387906975

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906975(C;T)
Make rs387906975(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position103049788
GeneCNNM2
is asnp
is mentioned by
dbSNPrs387906975
ebirs387906975
HLIrs387906975
Exacrs387906975
Varsomers387906975
Maprs387906975
PheGenIrs387906975
hapmaprs387906975
1000 genomesrs387906975
hgdprs387906975
ensemblrs387906975
gopubmedrs387906975
geneviewrs387906975
scholarrs387906975
googlers387906975
pharmgkbrs387906975
gwascentralrs387906975
openSNPrs387906975
23andMers387906975
23andMe allrs387906975
SNP Nexus

SNPshotrs387906975
SNPdbers387906975
MSV3drs387906975
GWAS Ctlgrs387906975
Max Magnitude0
ClinVar
Risk rs387906975(T;T)
Alt rs387906975(T;T)
Reference rs387906975(C;C)
Significance Pathogenic
Disease Hypomagnesemia 6
Variation info
Gene CNNM2
CLNDBN Hypomagnesemia 6, renal
Reversed 0
HGVS NC_000010.10:g.104809545C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023661.2,