Variant (rsID / SNP)

rs17324153

rs17324153 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCRN1. Location: chromosome 7, position 29,966,141. The table records no clinical significance for this variant.

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Reference-table entries

SCRN1Not classified

Variant type: missense_variant
Chromosome / position: 7:29966141
HGVS: NM_001145514.1,c.1073A>G,p.Gln358Arg
Allele change: Missense_Q270R

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.