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Variant (rsID / SNP)

rs2637777

FAT1

rs2637777 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT1. Location: chromosome 4, position 187,525,020. The table records no clinical significance for this variant.

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Reference-table entries

FAT1Not classified
Variant type
missense_variant
Chromosome / position
4:187525020
HGVS
NM_005245.4,c.10660T>G,p.Ser3554Ala
Allele change
Missense_S3554A

Associated conditions / phenotypes

Major Affective Disorder 5|Major Affective Disorder 1|Major Affective Disorder 6

Public references

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