Have questions? Visit https://www.reddit.com/r/SNPedia

rs879253778

From SNPedia

Orientationminus
Geno Mag Summary
(GTACAGG;GTACAGG) 0 common in clinvar
Make rs879253778(-;-)
Make rs879253778(-;GTACAGG)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position37914412
GeneSFRP4
is asnp
is mentioned by
dbSNPrs879253778
ebirs879253778
HLIrs879253778
Exacrs879253778
Varsomers879253778
Maprs879253778
PheGenIrs879253778
hapmaprs879253778
1000 genomesrs879253778
hgdprs879253778
ensemblrs879253778
gopubmedrs879253778
geneviewrs879253778
scholarrs879253778
googlers879253778
pharmgkbrs879253778
gwascentralrs879253778
openSNPrs879253778
23andMers879253778
23andMe allrs879253778
SNP Nexus

SNPshotrs879253778
SNPdbers879253778
MSV3drs879253778
GWAS Ctlgrs879253778
Max Magnitude0
ClinVar
Risk rs879253778(;)
Alt rs879253778(;)
Reference rs879253778(GTACAGG;GTACAGG)
Significance Pathogenic
Disease Pyle metaphyseal dysplasia
Variation info
Gene SFRP4
CLNDBN Pyle metaphyseal dysplasia
Reversed 1
HGVS NC_000007.13:g.37954014_37954020delCCTGTAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000234974.1,