Version: 8.0.0
Date: Tue Jan 28 2025
1 results
Allele/Variant Genes: HSPA1B (Hsa) Molecular Consequence: missense variant

(GRCh38)6:31827773C>T

(Homo sapiens)
Allele/Variant
Source: rs6457452
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31827773C>T