{{Rsnum
|rsid=137852813
|Chromosome=2
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SOS1
|position=39051202
|Gene_s=SOS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=182530
|variant=0003
|rsnum=137852813
}}{{ClinVar
|rsid=137852813
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=39278343
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SOS1:6654
|GENE_NAME=SOS1
|GENE_ID=6654
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000002.11:g.39278343A>C; NC_000002.11:g.39278343A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=182530.0003
|CLNSIG=5
|CLNCUI=C1853120
|CLNDBN=Noonan syndrome 4; Noonan's syndrome
|Disease=Noonan syndrome 4; Noonan's syndrome
|CLNACC=RCV000013730.21; RCV000038572.1; RCV000038571.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1124:C1853120:163955:610733:648; NBK1124:C0028326:163950:205824006
}}