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rs1057519419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519419(A;G)
Make rs1057519419(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position193125110
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs1057519419
dbSNP (classic)rs1057519419
ClinGenrs1057519419
ebirs1057519419
HLIrs1057519419
Exacrs1057519419
Gnomadrs1057519419
Varsomers1057519419
LitVarrs1057519419
Maprs1057519419
PheGenIrs1057519419
Biobankrs1057519419
1000 genomesrs1057519419
hgdprs1057519419
ensemblrs1057519419
geneviewrs1057519419
scholarrs1057519419
googlers1057519419
pharmgkbrs1057519419
gwascentralrs1057519419
openSNPrs1057519419
23andMers1057519419
23andMe allrs1057519419
SNPshotrs1057519419
SNPdbers1057519419
MSV3drs1057519419
GWAS Ctlgrs1057519419
Max Magnitude0
ClinVar
Risk rs1057519419(G;G)
Alt rs1057519419(G;G)
Reference Rs1057519419(A;A)
Significance Probable-Pathogenic
Disease Hyperparathyroidism 1
Variation info
Gene CDC73 LOC101929160
CLNDBN Hyperparathyroidism 1
Reversed 0
HGVS NC_000001.10:g.193094240A>G
CLNSRC
CLNACC RCV000417061.1,