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rs755007671

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755007671(A;A)
Make rs755007671(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position37912216
GeneSFRP4
is asnp
is mentioned by
dbSNPrs755007671
ebirs755007671
HLIrs755007671
Exacrs755007671
Varsomers755007671
Maprs755007671
PheGenIrs755007671
hapmaprs755007671
1000 genomesrs755007671
hgdprs755007671
ensemblrs755007671
gopubmedrs755007671
geneviewrs755007671
scholarrs755007671
googlers755007671
pharmgkbrs755007671
gwascentralrs755007671
openSNPrs755007671
23andMers755007671
23andMe allrs755007671
SNP Nexus

SNPshotrs755007671
SNPdbers755007671
MSV3drs755007671
GWAS Ctlgrs755007671
Max Magnitude0
ClinVar
Risk rs755007671(A;A)
Alt rs755007671(A;A)
Reference rs755007671(G;G)
Significance Pathogenic
Disease Pyle metaphyseal dysplasia
Variation info
Gene SFRP4
CLNDBN Pyle metaphyseal dysplasia
Reversed 0
HGVS NC_000007.13:g.37951818G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234991.1,