Variant (rsID / SNP)

rs10917051

rs10917051 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDLRAD2. Location: chromosome 1, position 22,141,206. The table records no clinical significance for this variant.

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Reference-table entries

LDLRAD2Not classified

Variant type: missense_variant
Chromosome / position: 1:22141206
HGVS: NM_001013693.3,c.401A>C,p.Asn134Thr
Allele change: Missense_N134T

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.