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rs199955107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199955107(A;A)
Make rs199955107(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position13492587
GenePTH
is asnp
is mentioned by
dbSNPrs199955107
dbSNP (old)rs199955107
ClinGenrs199955107
ebirs199955107
HLIrs199955107
Exacrs199955107
Gnomadrs199955107
Varsomers199955107
Maprs199955107
PheGenIrs199955107
Biobankrs199955107
1000 genomesrs199955107
hgdprs199955107
ensemblrs199955107
gopubmedrs199955107
geneviewrs199955107
scholarrs199955107
googlers199955107
pharmgkbrs199955107
gwascentralrs199955107
openSNPrs199955107
23andMers199955107
23andMe allrs199955107
SNPshotrs199955107
SNPdbers199955107
MSV3drs199955107
GWAS Ctlgrs199955107
Max Magnitude0
ClinVar
Risk rs199955107(A;A)
Alt rs199955107(A;A)
Reference Rs199955107(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTH
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.13514134G>A
CLNSRC
CLNACC RCV000421942.1,