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rs141156594

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs141156594(A;G)
Make rs141156594(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position70196537
GeneRTTN
is asnp
is mentioned by
dbSNPrs141156594
ebirs141156594
HLIrs141156594
Exacrs141156594
Varsomers141156594
Maprs141156594
PheGenIrs141156594
hapmaprs141156594
1000 genomesrs141156594
hgdprs141156594
ensemblrs141156594
gopubmedrs141156594
geneviewrs141156594
scholarrs141156594
googlers141156594
pharmgkbrs141156594
gwascentralrs141156594
openSNPrs141156594
23andMers141156594
23andMe allrs141156594
SNP Nexus

SNPshotrs141156594
SNPdbers141156594
MSV3drs141156594
GWAS Ctlgrs141156594
Max Magnitude0

[PMID 25305228] Differential susceptible loci expression in keloid and hypertrophic scars in the Chinese Han population

ClinVar
Risk rs141156594(C,G;C,G)
Alt rs141156594(C,G;C,G)
Reference rs141156594(A;A)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene RTTN
CLNDBN not specified
Reversed 0
HGVS NC_000018.9:g.67863773A>G
CLNSRC
CLNACC RCV000118227.2,