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rs387906960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906960(A;A)
Make rs387906960(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position41817156
GeneFKBP10
is asnp
is mentioned by
dbSNPrs387906960
ebirs387906960
HLIrs387906960
Exacrs387906960
Varsomers387906960
Maprs387906960
PheGenIrs387906960
hapmaprs387906960
1000 genomesrs387906960
hgdprs387906960
ensemblrs387906960
gopubmedrs387906960
geneviewrs387906960
scholarrs387906960
googlers387906960
pharmgkbrs387906960
gwascentralrs387906960
openSNPrs387906960
23andMers387906960
23andMe allrs387906960
SNP Nexus

SNPshotrs387906960
SNPdbers387906960
MSV3drs387906960
GWAS Ctlgrs387906960
Max Magnitude0
ClinVar
Risk rs387906960(A;A)
Alt rs387906960(A;A)
Reference rs387906960(G;G)
Significance Pathogenic
Disease Bruck syndrome 1
Variation info
Gene FKBP10
CLNDBN Bruck syndrome 1
Reversed 0
HGVS NC_000017.10:g.39973408G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023609.5,