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rs1057519948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519948(C;T)
Make rs1057519948(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position6387262
GeneRAC1
is asnp
is mentioned by
dbSNPrs1057519948
dbSNP (classic)rs1057519948
ClinGenrs1057519948
ebirs1057519948
HLIrs1057519948
Exacrs1057519948
Gnomadrs1057519948
Varsomers1057519948
LitVarrs1057519948
Maprs1057519948
PheGenIrs1057519948
Biobankrs1057519948
1000 genomesrs1057519948
hgdprs1057519948
ensemblrs1057519948
geneviewrs1057519948
scholarrs1057519948
googlers1057519948
pharmgkbrs1057519948
gwascentralrs1057519948
openSNPrs1057519948
23andMers1057519948
SNPshotrs1057519948
SNPdbers1057519948
MSV3drs1057519948
GWAS Ctlgrs1057519948
Max Magnitude0
ClinVar
Risk rs1057519948(T;T)
Alt rs1057519948(T;T)
Reference Rs1057519948(C;C)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Malignant melanoma of skin
Variation info
Gene RAC1
CLNDBN Malignant neoplasm of body of uterus Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Malignant melanoma of skin
Reversed 0
HGVS NC_000007.13:g.6426893C>T
CLNSRC
CLNACC RCV000427753.1, RCV000431469.1, RCV000434094.1, RCV000443782.1,