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rs757094189

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs757094189(C;C)
Make rs757094189(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39013522
GeneSOS1
is asnp
is mentioned by
dbSNPrs757094189
ebirs757094189
HLIrs757094189
Exacrs757094189
Varsomers757094189
Maprs757094189
PheGenIrs757094189
hapmaprs757094189
1000 genomesrs757094189
hgdprs757094189
ensemblrs757094189
gopubmedrs757094189
geneviewrs757094189
scholarrs757094189
googlers757094189
pharmgkbrs757094189
gwascentralrs757094189
openSNPrs757094189
23andMers757094189
23andMe allrs757094189
SNP Nexus

SNPshotrs757094189
SNPdbers757094189
MSV3drs757094189
GWAS Ctlgrs757094189
Max Magnitude0
ClinVar
Risk rs757094189(C;C)
Alt rs757094189(C;C)
Reference rs757094189(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.39240663T>C
CLNSRC
CLNACC RCV000171288.1,