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rs786200937

From SNPedia

Orientationplus
Geno Mag Summary
(GTAAATTT;GTAAATTT) 0 common in clinvar
Make rs786200937(-;-)
Make rs786200937(-;TAAATTTG)
Make rs786200937(TAAATTTG;TAAATTTG)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position109741499
GeneFIG4
is asnp
is mentioned by
dbSNPrs786200937
ebirs786200937
HLIrs786200937
Exacrs786200937
Varsomers786200937
Maprs786200937
PheGenIrs786200937
hapmaprs786200937
1000 genomesrs786200937
hgdprs786200937
ensemblrs786200937
gopubmedrs786200937
geneviewrs786200937
scholarrs786200937
googlers786200937
pharmgkbrs786200937
gwascentralrs786200937
openSNPrs786200937
23andMers786200937
23andMe allrs786200937
SNP Nexus

SNPshotrs786200937
SNPdbers786200937
MSV3drs786200937
GWAS Ctlgrs786200937
Max Magnitude0
ClinVar
Risk rs786200937(;)
Alt rs786200937(;)
Reference rs786200937(GTAAATTT;GTAAATTT)
Significance Pathogenic
Disease Yunis Varon syndrome not provided
Variation info
Gene FIG4
CLNDBN Yunis Varon syndrome not provided
Reversed 0
HGVS NC_000006.11:g.110062702_110062709delTAAATTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000043691.3, RCV000236453.1,