Variant (rsID / SNP)

rs6437353

rs6437353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR35. Location: chromosome 2, position 241,558,397. The table records no clinical significance for this variant.

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Reference-table entries

GPR35Not classified

Variant type: missense_variant
Chromosome / position: 2:241558397
HGVS: NM_001195381.3,c.38G>A,p.Arg13His
Allele change: Missense_R13H

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.