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rs397514674

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514674(A;A)
Make rs397514674(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position41817149
GeneFKBP10
is asnp
is mentioned by
dbSNPrs397514674
ebirs397514674
HLIrs397514674
Exacrs397514674
Varsomers397514674
Maprs397514674
PheGenIrs397514674
hapmaprs397514674
1000 genomesrs397514674
hgdprs397514674
ensemblrs397514674
gopubmedrs397514674
geneviewrs397514674
scholarrs397514674
googlers397514674
pharmgkbrs397514674
gwascentralrs397514674
openSNPrs397514674
23andMers397514674
23andMe allrs397514674
SNP Nexus

SNPshotrs397514674
SNPdbers397514674
MSV3drs397514674
GWAS Ctlgrs397514674
Max Magnitude0
ClinVar
Risk rs397514674(A,C;A,C)
Alt rs397514674(A,C;A,C)
Reference rs397514674(G;G)
Significance Pathogenic
Disease Bruck syndrome 1
Variation info
Gene FKBP10
CLNDBN Bruck syndrome 1
Reversed 0
HGVS NC_000017.10:g.39973401G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034360.7,