Variant (rsID / SNP)

rs11939575

rs11939575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT1. Location: chromosome 4, position 187,627,792. The table records no clinical significance for this variant.

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Reference-table entries

FAT1Not classified

Variant type: missense_variant
Chromosome / position: 4:187627792
HGVS: NM_005245.4,c.3190A>G,p.Arg1064Gly
Allele change: Missense_R1064G

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.