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rs1060499629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTAAGTGGCA;GTAAGTGGCA) 0 common in clinvar
Make rs1060499629(-;-)
Make rs1060499629(-;GTAAGTGGCA)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position241517172
GeneFH
is asnp
is mentioned by
dbSNPrs1060499629
dbSNP (old)rs1060499629
ClinGenrs1060499629
ebirs1060499629
HLIrs1060499629
Exacrs1060499629
Gnomadrs1060499629
Varsomers1060499629
LitVarrs1060499629
Maprs1060499629
PheGenIrs1060499629
Biobankrs1060499629
1000 genomesrs1060499629
hgdprs1060499629
ensemblrs1060499629
gopubmedrs1060499629
geneviewrs1060499629
scholarrs1060499629
googlers1060499629
pharmgkbrs1060499629
gwascentralrs1060499629
openSNPrs1060499629
23andMers1060499629
23andMe allrs1060499629
SNPshotrs1060499629
SNPdbers1060499629
MSV3drs1060499629
GWAS Ctlgrs1060499629
Max Magnitude0
ClinVar
Risk rs1060499629(-;-)
Alt rs1060499629(-;-)
Reference Rs1060499629(GTAAGTGGCA;GTAAGTGGCA)
Significance Pathogenic
Disease Hereditary leiomyomatosis and renal cell cancer
Variation info
Gene FH
CLNDBN Hereditary leiomyomatosis and renal cell cancer
Reversed 1
HGVS NC_000001.10:g.241680472_241680481delTGCCACTTAC
CLNSRC
CLNACC RCV000445611.1,