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Variant (rsID / SNP)

rs17603649

CCDC191

rs17603649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC191. Location: chromosome 3, position 113,737,568. The table records no clinical significance for this variant.

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Reference-table entries

CCDC191Not classified
Variant type
missense_variant
Chromosome / position
3:113737568
HGVS
NM_020817.2,c.1120C>T,p.Arg374Trp
Allele change
Missense_R352W

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.