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rs12628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs12628(C;C)
Make rs12628(C;T)
ReferenceGRCh37 37.1/131
Chromosome11
Position534242
GeneHRAS
is asnp
is mentioned by
dbSNPrs12628
ebirs12628
HLIrs12628
Exacrs12628
Varsomers12628
Maprs12628
PheGenIrs12628
hapmaprs12628
1000 genomesrs12628
hgdprs12628
ensemblrs12628
gopubmedrs12628
geneviewrs12628
scholarrs12628
googlers12628
pharmgkbrs12628
gwascentralrs12628
openSNPrs12628
23andMers12628
23andMe allrs12628
SNP Nexus

SNPshotrs12628
SNPdbers12628
MSV3drs12628
GWAS Ctlgrs12628
GMAF0.2971
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM190020
DescV-HA-RAS HARVEY RAT SARCOMA VIRAL ONCOGENE HOMOLOG; HRAS
Variant
Relatedalso
[PMID 22618666OA-icon.png] Association between HRAS rs12628 and rs112587690 polymorphisms with the risk of melanoma in the North American population


[PMID 16835863] Paternal bias in parental origin of HRAS mutations in Costello syndrome.


ClinVar
Risk rs12628(C;C)
Alt rs12628(C;C)
Reference rs12628(T;T)
Significance Non-pathogenic
Disease not specified Rasopathy
Variation info
Gene HRAS
CLNDBN not specified Rasopathy
Reversed 1
HGVS NC_000011.9:g.534242A>G
CLNSRC HGMD
CLNACC RCV000038468.6, RCV000149841.1,