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rs761095873

From SNPedia

Orientationplus
Make rs761095873(-;-)
Make rs761095873(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158666381
GeneGFM1, LXN
is asnp
is mentioned by
dbSNPrs761095873
ebirs761095873
HLIrs761095873
Exacrs761095873
Varsomers761095873
Maprs761095873
PheGenIrs761095873
hapmaprs761095873
1000 genomesrs761095873
hgdprs761095873
ensemblrs761095873
gopubmedrs761095873
geneviewrs761095873
scholarrs761095873
googlers761095873
pharmgkbrs761095873
gwascentralrs761095873
openSNPrs761095873
23andMers761095873
23andMe allrs761095873
SNP Nexus

SNPshotrs761095873
SNPdbers761095873
MSV3drs761095873
GWAS Ctlgrs761095873
Max Magnitude
ClinVar
Risk rs761095873(;)
Alt rs761095873(;)
Reference rs761095873(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GFM1 LXN
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158384170delT
CLNSRC
CLNACC RCV000196892.1,