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rs866141540

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs866141540(-;-)
Make rs866141540(-;GT)
Make rs866141540(GT;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position6096996
GeneFERMT1
is asnp
is mentioned by
dbSNPrs866141540
ebirs866141540
HLIrs866141540
Exacrs866141540
Varsomers866141540
Maprs866141540
PheGenIrs866141540
hapmaprs866141540
1000 genomesrs866141540
hgdprs866141540
ensemblrs866141540
gopubmedrs866141540
geneviewrs866141540
scholarrs866141540
googlers866141540
pharmgkbrs866141540
gwascentralrs866141540
openSNPrs866141540
23andMers866141540
23andMe allrs866141540
SNP Nexus

SNPshotrs866141540
SNPdbers866141540
MSV3drs866141540
GWAS Ctlgrs866141540
Max Magnitude0
ClinVar
Risk rs866141540(;)
Alt rs866141540(;)
Reference rs866141540(TG;TG)
Significance Pathogenic
Disease Kindler's syndrome
Variation info
Gene FERMT1
CLNDBN Kindler's syndrome
Reversed 0
HGVS NC_000020.10:g.6077643_6077644delTG
CLNSRC
CLNACC RCV000209882.1,