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rs371900329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371900329(C;T)
Make rs371900329(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position103458291
GeneCALHM1
is asnp
is mentioned by
dbSNPrs371900329
dbSNP (classic)rs371900329
ClinGenrs371900329
ebirs371900329
HLIrs371900329
Exacrs371900329
Gnomadrs371900329
Varsomers371900329
LitVarrs371900329
Maprs371900329
PheGenIrs371900329
Biobankrs371900329
1000 genomesrs371900329
hgdprs371900329
ensemblrs371900329
geneviewrs371900329
scholarrs371900329
googlers371900329
pharmgkbrs371900329
gwascentralrs371900329
openSNPrs371900329
23andMers371900329
23andMe allrs371900329
SNPshotrs371900329
SNPdbers371900329
MSV3drs371900329
GWAS Ctlgrs371900329
Max Magnitude0
ClinVar
Risk rs371900329(T;T)
Alt rs371900329(T;T)
Reference Rs371900329(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CALHM1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.105218048C>T
CLNSRC
CLNACC RCV000424150.1,