Variant (rsID / SNP)

rs4777035

rs4777035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGA11. Location: chromosome 15, position 68,605,169. The table records no clinical significance for this variant.

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Reference-table entries

ITGA11Not classified

Variant type: missense_variant
Chromosome / position: 15:68605169
HGVS: NM_001004439.2,c.2915C>T,p.Pro972Leu
Allele change: Missense_P972L

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.