Variant (rsID / SNP)

rs1131773

rs1131773 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SUSD3. Location: chromosome 9, position 95,840,256. The table records no clinical significance for this variant.

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Reference-table entries

SUSD3Not classified

Variant type: missense_variant
Chromosome / position: 9:95840256
HGVS: NM_145006.4,c.406A>G,p.Lys136Glu
Allele change: Missense_K136E

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.