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rs267607048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607048(A;G)
Make rs267607048(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position110964362
GeneSHOC2
is asnp
is mentioned by
dbSNPrs267607048
ebirs267607048
HLIrs267607048
Exacrs267607048
Varsomers267607048
Maprs267607048
PheGenIrs267607048
hapmaprs267607048
1000 genomesrs267607048
hgdprs267607048
ensemblrs267607048
gopubmedrs267607048
geneviewrs267607048
scholarrs267607048
googlers267607048
pharmgkbrs267607048
gwascentralrs267607048
openSNPrs267607048
23andMers267607048
23andMe allrs267607048
SNP Nexus

SNPshotrs267607048
SNPdbers267607048
MSV3drs267607048
GWAS Ctlgrs267607048
Max Magnitude0
ClinVar
Risk rs267607048(G;G)
Alt rs267607048(G;G)
Reference rs267607048(A;A)
Significance Other
Disease Noonan-like syndrome with loose anagen hair Rasopathy Noonan syndrome not provided
Variation info
Gene SHOC2
CLNDBN Noonan-like syndrome with loose anagen hair Rasopathy Noonan syndrome not provided
Reversed 0
HGVS NC_000010.10:g.112724120A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007223.7, RCV000149834.4, RCV000208379.1, RCV000213000.1,