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

rs730881020

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881020(A;A)
Make rs730881020(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position110964877
GeneSHOC2
is asnp
is mentioned by
dbSNPrs730881020
ebirs730881020
HLIrs730881020
Exacrs730881020
Varsomers730881020
Maprs730881020
PheGenIrs730881020
hapmaprs730881020
1000 genomesrs730881020
hgdprs730881020
ensemblrs730881020
gopubmedrs730881020
geneviewrs730881020
scholarrs730881020
googlers730881020
pharmgkbrs730881020
gwascentralrs730881020
openSNPrs730881020
23andMers730881020
23andMe allrs730881020
SNP Nexus

SNPshotrs730881020
SNPdbers730881020
MSV3drs730881020
GWAS Ctlgrs730881020
Max Magnitude0
ClinVar
Risk rs730881020(A;A)
Alt rs730881020(A;A)
Reference rs730881020(G;G)
Significance Pathogenic
Disease not specified Noonan-like syndrome with loose anagen hair
Variation info
Gene SHOC2
CLNDBN not specified Noonan-like syndrome with loose anagen hair
Reversed 0
HGVS NC_000010.10:g.112724635G>A
CLNSRC
CLNACC RCV000159111.2, RCV000169685.1,