Variant (rsID / SNP)

rs12442757

rs12442757 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGDCC4. Location: chromosome 15, position 65,689,267. The table records no clinical significance for this variant.

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Reference-table entries

IGDCC4Not classified

Variant type: missense_variant
Chromosome / position: 15:65689267
HGVS: NM_020962.3,c.902A>G,p.Asn301Ser
Allele change: Missense_N301S

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.